Antiviral beta-amino acid ester phosphodiamide compounds

ABSTRACT

Compounds of Formula I: 
                         
and their pharmaceutically acceptable salts are useful for the inhibition of HIV reverse transcriptase. The compounds may also be useful for the prophylaxis or treatment of infection by HIV and in the prophylaxis, delay in the onset or progression, and treatment of AIDS. The compounds and their salts can be employed as ingredients in pharmaceutical compositions, optionally in combination with other antiviral agents, immunomodulators, antibiotics or vaccines.

RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No. 62/203,265, filed Aug. 10, 2015. The aforementioned application to which this application claims priority is herein incorporated by reference in its entirety.

BACKGROUND OF THE INVENTION

The retrovirus designated human immunodeficiency virus (HIV), particularly the strains known as HIV type-1 (HIV-1) and type-2 (HIV-2), have been etiologically linked to the immunosuppressive disease known as acquired immunodeficiency syndrome (AIDS). HIV seropositive individuals are initially asymptomatic but typically develop AIDS related complex (ARC) followed by AIDS. Affected individuals exhibit severe immunosuppression which makes them highly susceptible to debilitating and ultimately fatal opportunistic infections. Replication of HIV by a host cell requires integration of the viral genome into the host cell's DNA. Since HIV is a retrovirus, the HIV replication cycle requires transcription of the viral RNA genome into DNA via an enzyme known as reverse transcriptase (RT).

Reverse transcriptase has three known enzymatic functions: The enzyme acts as an RNA-dependent DNA polymerase, as a ribonuclease, and as a DNA-dependent DNA polymerase. In its role as an RNA-dependent DNA polymerase, RT transcribes a single-stranded DNA copy of the viral RNA. As a ribonuclease, RT destroys the original viral RNA and frees the DNA just produced from the original RNA. During the viral RNA-dependent polymerization process, RT's ribonuclease activity is required for removing RNA and leaving the polypurine tract preserved for initiation of DNA-dependent polymerization. As a DNA-dependent DNA polymerase, RT makes a second, complementary DNA strand using the first DNA strand as a template. The two strands form double-stranded DNA, which is integrated into the host cell's genome by HIV integrase.

It is known that compounds that inhibit enzymatic functions of HIV RT will inhibit HIV replication in infected cells. These compounds are useful in the treatment of HIV infection in humans. There are two classes of RT inhibitors: one is non-nucleoside active site competitive RT inhibitors (NNRTIs), such as efavirenz (EFV), nevirapine (NVP), etravirine (ETR), and rilpivirine (RPV), and the other is active site RT inhibitors which include nucleoside reverse transcriptase inhibitors (NsRTIs) and nucleotide reverse transcriptase inhibitors (NtRTIs), collectively referred to as NRTIs. Examples of NsRTI's include 3′-azido-3′-deoxythymidine (AZT), 2′,3′-dideoxyinosine (ddI), 2′,3′-dideoxycytidine (ddC), 2′,3′-didehydro-2′,3′-dideoxythymidine (d4T), 2′,3′-dideoxy-3′-thiacytidine (3TC), abacavir, and emtricitabine. Examples of NtRTIs include tenofovir (TFV, also known as PMPA, 9-(2-phosphonyl-methoxypropyl)adenine), tenofovir disoproxil fumarate (VIREADO, U.S. Pat. No. 5,977,089, U.S. Pat. No. 5,935,946) and tenofovir alafenamide fumarate (U.S. Pat. Nos. 7,390,791, 8,754,065).

TFV belongs to a class of HIV anti-retroviral (ARV) agents known as nucleotide analog reverse transcriptase inhibitors (NRTIs). Tenofovir is a monophosphonate:

After being taken up by cells, TFV is first converted to tenofovir-monophosphate (TFV-MP) by adenosine monophosphate kinase and then to the active antiviral tenofovir-diphosphate (TFV-DP) by 5′-nucleoside diphosphate kinase.

TFV-DP inhibits HIV DNA synthesis by competing with the natural substrate, deoxyadenosine triphosphate, for incorporation into the complementary DNA strand by HIV reverse transcriptase; following incorporation, TFV acts as a chain terminator due to lack of a 3′-hydroxyl group that is required for addition of the next nucleotide. TFV has poor cellular permeability and thus has limited bioavailability. Tenofovir disoproxil fumarate (TDF) is approved for treating HIV infection and is marketed by Gilead under the trade name VIREAD™. The disoproxil prodrug improves cell permeability and absorption after oral dosing, with the pro-moiety being cleaved rapidly after absorption to yield the parent TFV. As a result, the circulating level of TFV is much higher than that of TDF. Tenofovir alafenamide fumarate (TAF) is currently approved by the USFDA as an active ingredient in combination with additional ARVs for treating HIV infection in the pharmaceutical products GENVOYA®, ODEFSEY® and DESCOVY®.

While each of the foregoing drugs is effective in treating HIV infection and AIDS, there remains a need to develop additional HIV antiviral drugs including additional RT inhibitors. A particular problem is the development of mutant HIV strains that are resistant to the known inhibitors. The use of RT inhibitors to treat AIDS often leads to viruses that are less sensitive to the inhibitors. This resistance is typically the result of mutations that occur in the reverse transcriptase segment of the pol gene. The continued use of antiviral compounds to prevent HIV infection will inevitably result in the emergence of new resistant strains of HIV. Accordingly, there is a particular need for new RT inhibitors that are effective against mutant HIV strains.

SUMMARY OF THE INVENTION

The present invention is directed to beta-amino acid ester phosphodiamide prodrugs of tenofovir and their use in the inhibition of nucleotide reverse transcriptase. In addition to the use of said compounds in the inhibition of HIV reverse transcriptase, the invention is also directed to the use of said compounds for prophylaxis of infection by HIV, the treatment of infection by HIV, and the prophylaxis, treatment, and/or delay in the onset or progression of AIDS and/or ARC.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is directed to compounds of structural Formula I:

or pharmaceutically acceptable salt thereof, wherein: R¹ and R² are each independently selected from (a) H, (b) (c) —C₁₋₄alkyl substituted with —OH, —SH, —SCH₃, —NH₂ or NH—C(═NH)—NH₂, (d) —CH₂-phenyl, (e) —CH₂-phenol, —(CH₂)₁₋₂—COOH, (g) —(CH₂)₁₋₂—CONH₂, (h) —CH₂-1H-indole, (i) —CH₂-imidazole, (j) aryl (for example but not limited to phenyl or naphthyl) or (k) heteroaryl (for example but not limited to pyridine); R3 is

-   -   (a) —C₁₋₁₀alkyl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(10a), —SH, —NR¹¹R¹², —C₃₋₆cycloalkyl or         spiro-C₃₋₆cycloalkyl,     -   (b) —CH₂-phenyl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (c) —C₃₋₈cycloalkyl unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (d) aryl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (e) —C₁₋₅alkyl-X—C₁₋₅alkyl wherein X is O, S or NH,     -   (f) heteroaryl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl, or     -   (g) a heterocyclic ring unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl;         R^(A) is an L-amino acid ester residue of formula (i), a D-amino         acid ester residue of formula (ii), a glycine ester residue of         formula (iii), a geminally di-substituted amino acid ester         residue of formula (iv), a beta amino acid ester residue of         formula (v), or an L-proline ester residue of formula (vi):

R⁴ is (a) —C₁₋₄alkyl, (b) —C₁₋₄alkyl substituted with —OH, —SH, —SCH₃, —NH₂, —NH—C(NH)—NH₂, (c) —CH₂-phenyl, (d) —CH₂-phenol, (e) —(CH₂)₁₋₂—COOH, (f) —(CH₂)₁₋₂—CONH₂, (g) —CH₂-1H-indole, (h) —CH₂-imidazole, (i) aryl (for example but not limited to phenyl or naphthyl) or (j) heteroaryl (for example but not limited to pyridine); R⁵ and R⁶ are each independently selected from (a) —C₁₋₄alkyl, (b) —C₁₋₄ alkyl substituted with —OH, —SH, —SCH₃, —NH₂, —NH—C(═NH)—NH₂, (c) —CH₂-phenyl, (d) —CH₂-phenol, (e) —(CH₂)₁₋₂—COOH, (f) —(CH₂)₁₋₂—CONH₂, (g) —CH₂-1H-indole, (h) —CH₂-imidazole, (i) aryl (for example but not limited to phenyl or naphthyl) or (j) heteroaryl (for example but not limited to pyridine); or R⁵ and R⁶ are joined together with the carbon to which they are both attached to form —C₃₋₆cycloalkyl or a 4 to 6-membered heterocyclic ring; R⁷ and R⁸ are each independently selected from (a) H, (b) (c) —C₁₋₄alkyl substituted with —OH, —SH, —SCH₃, —NH₂ or —NH—C(═NH)—NH₂, (d) —CH₂-phenyl, (e) —CH₂-phenol, (f) —(CH₂)₁₋₂—COOH, (g) —(CH₂)₁₋₂—CONH₂, (h) —CH₂-1H-indole, (i) —CH₂-imidazole, (j) aryl (for example but not limited to phenyl or naphthyl) or (k) heteroaryl (for example but not limited to pyridine); R⁹ is

-   -   (a) —C₁₋₁₀ alkyl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(10b), —SH, —NR¹³R¹⁴, —C₃₋₆cycloalkyl or         spiro-C₃₋₆cycloalkyl,     -   (b) —CH₂-phenyl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (c) —C₃₋₈cycloalkyl unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (d) aryl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (e) —C₁₋₅alkyl-X—C₁₋₅alkyl wherein X is O, S or NH;     -   (f) heteroaryl unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl, or     -   (g) a heterocyclic ring unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl;         R^(10a) and R^(10b) are each independently selected from —H or         —C₃₋₆cycloalkyl;         R¹¹ and R¹² are each independently selected from H, —C₁₋₃alkyl         or —C₃₋₆cycloalkyl;         R¹³ and R¹⁴ are each independently selected from H, —C₁₋₃ alkyl         or —C₃₋₆cycloalkyl; and         R^(15a) and R^(15b) are each independently selected from H,         —C₁₋₃alkyl or —C₃₋₆cycloalkyl.

In an embodiment of this invention are compounds of Formula I or the pharmaceutically acceptable salts thereof, wherein R^(A) is formula (i), referred to herein as compounds of Formula I-i.

In an embodiment of this invention are compounds of Formula I or the pharmaceutically acceptable salts thereof, wherein R^(A) is formula (ii), referred to herein as compounds of Formula I-ii.

In an embodiment of this invention are compounds of Formula I or the pharmaceutically acceptable salts thereof, wherein R^(A) is formula (iii), referred to herein as compounds of Formula I-iii.

In an embodiment of this invention are compounds of Formula I or the pharmaceutically acceptable salts thereof, wherein R^(A) is formula (iv), referred to herein as compounds of Formula I-iv.

In an embodiment of this invention are compounds of Formula I or the pharmaceutically acceptable salts thereof, wherein R^(A) is formula (v), referred to herein as compounds of Formula I-v.

In an embodiment of this invention are compounds of Formula I or the pharmaceutically acceptable salts thereof, wherein R^(A) is formula (vi), referred to herein as compounds of Formula I-vi.

In Embodiment 1 of this invention are compounds of Formula I, I-i, I-ii, I-iii, I-iv, I-v or I-vi, or Embodiment 2, 2a, 3, 4, 5, 6, 6a or 7, or a class thereof, or the pharmaceutically acceptable salts thereof, wherein R¹ is H or —C₁₋₄alkyl and R² is H or —C₁₋₄alkyl. In a class thereof, one of R¹ and R² is H, and the other is H or —C₁₋₄alkyl; and in a sub-class thereof one of R¹ and R² is H, and the other is —C₁₋₄alkyl, for example methyl or i-propyl.

In Embodiment 2 of this invention are compounds of Formula I, I-i, I-ii, I-iii, I-iv, I-v or I-vi or Embodiment 1, or the pharmaceutically acceptable salts thereof, wherein R³ is

-   -   (a) —C₁₋₈ alkyl, —CH₂CH₂OH, —CH₂CH₂CH₂OH, —CH₂CH₂SH,         —CH₂CH₂CH₂SH, —CH₂CH₂NH₂, —CH₂CH₂CH₂NH₂,     -   (b) —CH₂-phenyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (c) —C₃₋₆cycloalkyl, unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (d) phenyl or naphthyl, each unsubstituted or substituted with         one to three substituents independently selected from fluoro,         chloro, bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (e) —CH₂CH₂OCH₃, —CH₂CH₂CH₂OCH₃, —CH₂CH₂SCH₃, —CH₂CH₂CH₂SCH₃,         —CH₂CH₂NHCH₃, —CH₂CH₂CH₂NHCH₃,     -   (f) pyridyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15a), —NR¹¹R¹² or —C₁₋₃alkyl, or     -   (g) piperidinyl, pyrrolidinyl, tetrahydrofuranyl, or         tetrahydropyranyl, each unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl.         In a class of Embodiment 2, referred to as Embodiment 2a, R³ is         —C₁₋₈ alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl,         and in a sub-class thereof, R³ is —C₃₋₈alkyl, for example         i-propyl.

In Embodiment 3 of this invention are compounds of Formula I, I-i or I-ii or Embodiment 1, 2 or 2a, or the pharmaceutically acceptable salts thereof, wherein R⁴ is —C₁₋₄alkyl and in a sub-class thereof. R⁴ is —CH₃.

In Embodiment 4 of this invention are compounds of Formula I or I-iv or Embodiment 1 or 2, or the pharmaceutically acceptable salts thereof, wherein R⁵ and R⁶ are each independently selected from —CH₃, —CH₂CH₃, —C₃alkyl or —C₄alkyl. In another class of Embodiment 4, R⁵ and R⁶ are both the same atom moiety which is selected from —CH₃, —CH₂CH₃, —C₃alkyl or —C₄alkyl; and in a sub-class thereof. R⁵ and R⁶ are both —CH₃.

In Embodiment 5 of this invention are compounds of Formula I or I-v or Embodiment 1 or 2, or the pharmaceutically acceptable salts thereof, wherein R⁷ is H or —C₁₋₄alkyl and R⁸ is H or —C₁₋₄alkyl. In a class thereof, one of R⁷ and R⁸ is H, and the other is H or —C₁₋₄alkyl.

In Embodiment 6 of this invention are compounds of Formula I, I-i, I-ii, I-iii, I-iv, I-v or I-vi or Embodiment 1, 2 or 2a, or the pharmaceutically acceptable salts thereof, wherein R⁹ is

-   -   (a) —C₁₋₈ alkyl, —CH₂CH₂OH, —CH₂CH₂CH₂OH, —CH₂CH₂SH,         —CH₂CH₂CH₂SH, —CH₂CH₂NH₂, —CH₂CH₂CH₂NH₂,     -   (b) —CH₂-phenyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (c) —C₃₋₆cycloalkyl, unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (d) phenyl or naphthyl, each unsubstituted or substituted with         one to three substituents independently selected from fluoro,         chloro, bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (e) —CH₂CH₂OCH₃, —CH₂CH₂CH₂OCH₃, —CH₂CH₂SCH₃, —CH₂CH₂CH₂SCH₃,         —CH₂CH₂NHCH₃, —CH₂CH₂CH₂NHCH₃,     -   (f) pyridyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl, or     -   (g) piperidinyl, pyrrolidinyl, tetrahydrofuranyl, or         tetrahydropyranyl, each unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl.         In a class of Embodiment 6, referred to as Embodiment 6a, R⁹ is         —C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl,         and in a sub-class thereof, R⁹ is —C₃₋₈alkyl, cyclobutyl,         cyclopentyl or cyclohexyl.

In Embodiment 7 of this invention are compounds of Formula I, or a pharmaceutically acceptable salt thereof, wherein:

R¹ is H or —C₁₋₄alkyl;

R² is H or —C₁₋₄alkyl;

R³ is

-   -   (a) —C₁₋₄alkyl, —CH₂CH₂OH, —CH₂CH₂CH₂OH, —CH₂CH₂SH,         —CH₂CH₂CH₂SH, —CH₂CH₂NH₂, —CH₂CH₂CH₂NH₂,     -   (b) —CH₂-phenyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (c) —C₃₋₆cycloalkyl, unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (d) phenyl or naphthyl, each unsubstituted or substituted with         one to three substituents independently selected from fluoro,         chloro, bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl,     -   (e) —CH₂CH₂OCH₃, —CH₂CH₂CH₂OCH₃, —CH₂CH₂SCH₃, —CH₂CH₂CH₂SCH₃,         —CH₂CH₂NHCH₃, —CH₂CH₂CH₂NHCH₃,     -   (f) pyridyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl, or     -   (g) piperidinyl, pyrrolidinyl, tetrahydrofuranyl, or         tetrahydropyranyl, each unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15a), —SH, —NR¹¹R¹² or —C₁₋₃alkyl;         R⁴ is C₁₋₄alkyl;         R⁵ and R⁶ are both the same moiety which is selected from CH₃,         —CH₂CH₃, —C₃alkyl or —C₄alkyl;         R⁷ is H or —C₁₋₄alkyl and R⁸ is H or —C₁₋₄alkyl;         R⁹ is     -   (a) C₁₋₈alkyl, —CH₂CH₂OH, —CH₂CH₂CH₂OH, —CH₂CH₂SH, —CH₂CH₂CH₂SH,         —CH₂CH₂NH₂, —CH₂CH₂CH₂NH₂,     -   (b) —CH₂-phenyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (c) —C₃₋₆cycloalkyl, unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (d) phenyl or naphthyl, each unsubstituted or substituted with         one to three substituents independently selected from fluoro,         chloro, bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl,     -   (e) —CH₂CH₂OCH₃, —CH₂CH₂CH₂OCH₃, —CH₂CH₂SCH₃, —CH₂CH₂CH₂SCH₃,         —CH₂CH₂NHCH₃, —CH₂CH₂CH₂NHCH₃,     -   (f) pyridyl, unsubstituted or substituted with one to three         substituents independently selected from fluoro, chloro, bromo,         —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl, or     -   (g) piperidinyl, pyrrolidinyl, tetrahydrofuranyl, or         tetrahydropyranyl, each unsubstituted or substituted with one to         three substituents independently selected from fluoro, chloro,         bromo, —OR^(15b), —SH, —NR¹³R¹⁴ or —C₁₋₃alkyl;         and the remaining variables are as defined in Formula I.

In Embodiment 8 of this invention are compounds of Formula I, I-i, I-iv, I-v or I-vi, or a pharmaceutically acceptable salt thereof, wherein

one of R¹ and R² is H, and the other is —C₁₋₄alkyl; and

R³ is is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl,

or R³ is i-propyl.

In Embodiment 9 of this invention are compounds of Embodiment 8 having Formula I or I-i, or a pharmaceutically acceptable salt thereof, wherein

R⁴ is C₁₋₄alkyl or R⁴ is methyl; and

R⁹ is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, or R⁹ is C₃₋₈alkyl.

In Embodiment 10 of this invention are compounds of Embodiment 8 having Formula I or I-i, or a pharmaceutically acceptable salt thereof, wherein

R⁴ is C₁₋₄alkyl or R⁴ is methyl; and

R⁹ —C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, or R⁹ is C₃₋₈alkyl.

In Embodiment 11 of this invention are compounds of Embodiment 8 having Formula I or I-iii, or a pharmaceutically acceptable salt thereof, wherein

R⁹ is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, or R⁹ is C₃₋₈alkyl.

In Embodiment 12 of this invention are compounds of Embodiment 8 having Formula I or I-iv, or a pharmaceutically acceptable salt thereof, wherein

R⁵ and R⁶ are both the same atom moiety which is selected from —CH₃, —CH₂CH₃, —C₃alkyl or —C₄alkyl, or R⁵ and R⁶ are both —CH₃; and

R⁹ is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, or R⁹ is C₃₋₈alkyl.

In Embodiment 13 of this invention are compounds of Formula I or I-v, or a pharmaceutically acceptable salt thereof, wherein

R¹ is H or —C₁₋₄alkyl; R² is H or —C₁₋₄alkyl;

R7 is H or —C₁₋₄alkyl; R⁸ is H or —C₁₋₄alkyl;

R³ is is —C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, or R³ is i-propyl; and

R⁹ is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, or R⁹ is C₃₋₈alkyl.

In Embodiment 14 of this invention are compounds of Embodiment 8 having Formula I or I-vi, or a pharmaceutically acceptable salt thereof, wherein

R⁹ is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, or R⁹ is C₃₋₈alkyl.

In Embodiment 15 of this invention are compounds of Formula I, or a pharmaceutically acceptable salt thereof, wherein:

one of R¹ and R² is H, and the other is H or —C₁₋₄alkyl;

R³ is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl;

R⁴ is CH₃;

R⁵ and R⁶ are both —CH₃;

R⁷ is H or —C₁₋₄alkyl; R⁸ is H or —C₁₋₄alkyl;

R⁹ is C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; and the remaining variables are as defined in Formula I.

In Embodiment 16 of this invention are compounds of Formula I, or a pharmaceutically acceptable salt thereof, wherein:

one of R¹ and R² is H, and the other is methyl or i-propyl;

R³ is C₃₋₈alkyl, or R³ is i-propyl;

R⁴ is CH₃;

R⁵ and R⁶ are both —CH₃;

R⁷ is H or —C₁₋₄alkyl; R⁸ is H or —C₁₋₄alkyl; and

R⁹ is C₃₋₈alkyl, cyclobutyl, cyclopentyl or cyclohexyl;

and the remaining variables are as defined in Formula I.

Reference to the compounds of Formula I herein encompasses the compounds of Formula I and all embodiments, classes and sub-classes thereof. The compounds of the invention encompass compounds of Formula I and salts thereof when such salts are possible, including pharmaceutically acceptable salts.

As used herein, “alkyl” refers to both branched- and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms in a specified range. For example the term “C₁₋₁₀ alkyl” means linear or branched chain alkyl groups, including all possible isomers, having 1, 2, 3, 4, 5, 7, 8, 9 or 10 carbon atoms, and includes each of the decyl, nonyl, octyl, heptyl, hexyl and pentyl isomers as well as n-, iso-, sec- and tert-butyl (butyl, s-butyl, i-butyl, t-butyl; Bu=butyl, collectively “—C₄alkyl”), n- and iso-propyl (propyl, i-propyl, Pr=propyl, collectively “—C₃alkyl”), ethyl (Et) and methyl (Me). “C₁₋₄alkyl” has 1, 2, 3 or 4 carbon atoms, and includes each of n-, iso-, sec- and tert-butyl, n- and i-propyl, ethyl and methyl.

“Cycloalkyl” refers to a cyclized alkyl ring having the indicated number of carbon atoms in a specified range. Thus, for example, “C₃₋₈ cycloalkyl” encompasses each of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyloheptyl and cyclooctyl. “C₃₋₆cycloalkyl” encompasses each of cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. When cycloalkyl is a substituent on an alkyl group in a compound of Formula I, the cycloalkyl substituent can be bonded to any available carbon in the alkyl group. The following are illustrations of —C₃₋₆cycloalkyl substituents wherein the substituent is cyclopropyl in bold:

“Spiro-C₃₋₆cycloalkyl” refers to a cycloalkyl ring bonded to a non-terminal carbon atom wherein the non-terminal carbon atom is shared with the cycloalkyl group. Spiro-C₃₋₆cycloalkyl encompasses each of spiro-cyclopropyl, spiro-cyclobutyl, spiro-cyclopentyl and spiro-cyclohexyl. The following is an illustration of a spiro-C₃₋₆cycloalkyl substituent wherein the substituent is spiro-cyclopropyl in bold:

Examples of —C₁₋₅alkyl-X—C₁₋₅alkyl groups include, but are not limited to, —CH₂CH₂OCH₃, —CH₂CH₂CH₂OCH₃, —CH₂CH₂SCH₃, —CH₂CH₂CH₂SCH₃, —CH₂CH₂NHCH₃ or —CH₂CH₂CH₂NHCH₃.

“Aryl” refers to (i) phenyl, (ii) 9- or 10-membered bicyclic, fused carbocylic ring systems in which at least one ring is aromatic, and (iii) 11- to 14-membered tricyclic, fused carbocyclic ring systems in which at least one ring is aromatic. Suitable aryls include, for example, substituted and unsubstituted phenyl and substituted and unsubstituted naphthyl. An aryl of particular interest is unsubstituted or substituted phenyl.

“Heteroaryl” refers to (i) a 5- or 6-membered heteroaromatic ring containing from 1 to 4 heteroatoms independently selected from N, O and S, wherein each N is optionally in the form of an oxide, and (ii) a 9- or 10-membered bicyclic fused ring system, wherein the fused ring system of (ii) contains from 1 to 6 heteroatoms independently selected from N, O and S, wherein each ring in the fused ring system contains zero, one or more than one heteroatom, at least one ring is aromatic, each N is optionally in the form of an oxide, and each S in a ring which is not aromatic is optionally S(O) or S(O)₂. Suitable 5- and 6-membered heteroaromatic rings include, for example, pyridyl, 3-fluroropyridyl, 4-fluoropyridyl, 3-methoxypyridyl, 4-methoxypyridyl, pyrrolyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl, thienyl, furanyl, imidazolyl, pyrazolyl, triazolyl (i.e., 1,2,3-triazolyl or 1,2,4-triazolyl), tetrazolyl, oxazolyl, isooxazolyl, oxadiazolyl (i.e., the 1,2,3-, 1,2,4-, 1,2,5-(furazanyl), or 1,3,4-isomer), oxatriazolyl, thiazolyl, isothiazolyl, and thiadiazolyl. Suitable 9- and 10-membered heterobicyclic, fused ring systems include, for example, benzofuranyl, indolyl, indazolyl, naphthyridinyl, isobenzofuranyl, benzopiperidinyl, benzisoxazolyl, benzoxazolyl, chromenyl, quinolinyl, isoquinolinyl, isoindolyl, benzopiperidinyl, benzofuranyl, imidazo[1,2-a]pyridinyl, benzotriazolyl, indazolyl, indolinyl, and isoindolinyl. A class of heteroaryls includes unsubstituted or substituted pyridyl or pyrimidyl, and particularly unsubstituted or substituted pyridyl.

The term “heterocyclic ring” refers to (i) a saturated 4- to 7-membered cyclized ring and (ii) an unsaturated, non-aromatic 4 to 7-membered cyclized ring comprised of carbon atoms and 1-4 heteratoms independently selected from O, N and S. Heterocyclic rings within the scope of this invention include, for example, azetidinyl, piperidinyl, morpholinyl, thiomorpholinyl, thiazolidinyl, isothiazolidinyl, oxazolidinyl, isoxazolidinyl, pyrrolidinyl, imidazolidinyl, piperazinyl, tetrahydrofuranyl, tetrahydrothienyl, pyrazolidinyl, hexahydropyrimidinyl, thiazinanyl, thiazepanyl, azepanyl, diazepanyl, tetrahydropyranyl, tetrahydrothiopyranyl, and dioxanyl. Examples of 4- to 7-membered, unsaturated, non-aromatic heterocyclic rings within the scope of this invention include mono-unsaturated heterocyclic rings corresponding to the saturated heterocyclic rings listed in the preceding sentence in which a single bond is replaced with a double bond (e.g., a carbon-carbon single bond is replaced with a carbon-carbon double bond). A class of heterocyclic rings are 4 to 6-membered saturated monocyclic rings comprised of carbon atoms and 1 or 2 heteroatoms, wherein the heteroatoms are selected from N, O and S. Examples of 4 to 6 membered heterocyclic rings include but are not limited to, azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, tetrahydrofuranyl, tetrahydropyranyl and tetrahydrothiopyranyl, and a sub-class thereof is piperidinyl, pyrrolidinyl, tetrahydrofuranyl or tetrahydropyranyl. The following is an illustration of R⁵ and R⁶ when they are joined together to form a heterocyclic ring:

With respect to substituents on a molecule, “geminally” or “geminal” refers to two substituents, which may be the same or different, on one carbon.

It is understood that the specific rings and ring systems suitable for use in the present invention are not limited to those listed in the preceding paragraphs. These rings and ring systems are merely representative.

As would be recognized by one of ordinary skill in the art, certain compounds of the present invention may be able to exist as tautomers. All tautomeric forms of these compounds, whether isolated individually or in mixtures, are within the scope of the present invention. For example, in instances where an —OH substituent is permitted on a heteroaromatic ring and ketoenol tautomerism is possible, it is understood that the substituent might in fact be present, in whole or in part, in the oxo (═O) form.

A “stable” compound is a compound which can be prepared and isolated and whose structure and properties remain or can be caused to remain essentially unchanged for a period of time sufficient to allow use of the compound for the purposes described herein (e.g., therapeutic or prophylactic administration to a subject). The compounds of the present invention are limited to stable compounds embraced by Formula I and its embodiments. For example, certain moieties as defined in Formula I may be unsubstituted or substituted, and the latter is intended to encompass substitution patterns (i.e., number and kind of substituents) that are chemically possible for the moiety and that result in a stable compound.

Each compound of Formula I is comprised of a phosphodiamide amino acid ester having a defined (R) chiral center in the alkyl-ether linking group connecting the nucleobase to the phosphodiamide as shown in Formula I, and may have one or more additional chiral centers depending on substituent selection. For example, each of Examples 6-28 herein also has an assymetric phosphorus center. Accordingly, a compound of Formula I may have multiple chiral centers (also referred to as asymmetric or stereogenic centers. This invention encompasses compounds having either the (R) or (S) stereo-configuration at a phosphorus assymetric center and at any additional assymetric centers that may be present in a compound of Formula I, as well as stereo-isomeric mixtures thereof.

This invention includes individual diastereomers, particularly epimers, i.e., compounds having the same chemical formula but which differ in the spatial arrangement around a single atom. This invention also includes mixtures of diastereomers, particularly mixtures of epimers, in all ratios. Embodiments of this invention also include a mixture of epimers enriched with 51% or more of one of the epimers, including for example 60% or more, 70% or more, 80% or more, or 90% or more of one epimer. A single epimer is preferred. An individual or single epimer refers to an epimer obtained by chiral synthesis and/or using generally known separation and purification techniques, and which may be 100% of one epimer or may contain small amounts (e.g., 10% or less) of the opposite epimer. Thus, individual diasteromers are a subject of the invention in pure form, both as levorotatory and as dextrorotatory antipodes, in the form of racemates and in the form of mixtures of the two diasteromers in all ratios. In the case of a cis/trans isomerism the invention includes both the cis form and the trans form as well as mixtures of these forms in all ratios.

The preparation of individual stereoisomers can be carried out, if desired, by separation of a mixture by customary methods, for example by chromatography or crystallization, by the use of stereochemically uniform starting materials for the synthesis or by stereoselective synthesis. Optionally a derivatization can be carried out before a separation of stereoisomers. The separation of a mixture of stereoisomers can be carried out at an intermediate step during the synthesis of a compound of Formula I or it can be done on a final racemic product. Absolute stereochemistry may be determined by X-ray crystallography of crystalline products or crystalline intermediates which are derivatized, if necessary, with a reagent containing a stereogenic center of known configuration. Alternatively, absolute stereochemistry may be determined by Vibrational Circular Dichroism (VCD) spectroscopy analysis. The present invention includes all such isomers, as well as salts, solvates (which includes hydrates) and solvated salts of such racemates, enantiomers, diastereomers and tautomers and mixtures thereof.

The atoms in a compound of Formula I may exhibit their natural isotopic abundances, or one or more of the atoms may be artificially enriched in a particular isotope having the same atomic number, but an atomic mass or mass number different from the atomic mass or mass number predominantly found in nature. The present invention is meant to include all suitable isotopic variations of the compounds of Formula I; for example, different isotopic forms of hydrogen (H) include protium (¹H) and deuterium (²H). Protium is the predominant hydrogen isotope found in nature. Enriching for deuterium may afford certain therapeutic advantages, such as increasing in vivo half-life or reducing dosage requirements, or may provide a compound useful as a standard for characterization of biological samples. Isotopically-enriched compounds of Formula I can be prepared without undue experimentation by conventional techniques well known to those skilled in the art or by processes analogous to those described in the Schemes and Examples herein using appropriate isotopically-enriched reagents and/or intermediates.

The compounds can be administered in the form of pharmaceutically acceptable salts. The term “pharmaceutically acceptable salt” refers to a salt which is not biologically or otherwise undesirable (e.g., is neither toxic nor otherwise deleterious to the recipient thereof). Since the compounds of Formula I contain by definition at least one basic group, the invention includes the corresponding pharmaceutically acceptable salts. When the compounds of Formula I contain one or more acidic groups, the invention also includes the corresponding pharmaceutically acceptable salts. Thus, the compounds of Formula I that contain acidic groups (e.g., —COOH) can be used according to the invention as, for example but not limited to, alkali metal salts, alkaline earth metal salts or as ammonium salts. Examples of such salts include but are not limited to sodium salts, potassium salts, calcium salts, magnesium salts or salts with ammonia or organic amines such as, for example, ethylamine, ethanolamine, triethanolamine or amino acids. Compounds of Formula I, which contain one or more basic groups, i.e. groups which can be protonated, can be used according to the invention in the form of their acid addition salts with inorganic or organic acids as, for example but not limited to, salts with hydrogen chloride, hydrogen bromide, phosphoric acid, sulfuric acid, nitric acid, benzenesulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acids, oxalic acid, acetic acid, trifluoroacetic acid, tartaric acid, lactic acid, salicylic acid, benzoic acid, formic acid, propionic acid, pivalic acid, diethylacetic acid, malonic acid, succinic acid, pimelic acid, fumaric acid, maleic acid, malic acid, sulfaminic acid, phenylpropionic acid, gluconic acid, ascorbic acid, isonicotinic acid, citric acid, adipic acid, etc. If the compounds of Formula I simultaneously contain acidic and basic groups in the molecule the invention also includes, in addition to the salt forms mentioned, inner salts or betaines (zwitterions). Salts can be obtained from the compounds of Formula I by customary methods which are known to the person skilled in the art, for example by combination with an organic or inorganic acid or base in a solvent or dispersant, or by anion exchange or cation exchange from other salts. The present invention also includes all salts of the compounds of Formula I which, owing to low physiological compatibility, are not directly suitable for use in pharmaceuticals but which can be used, for example, as intermediates for chemical reactions or for the preparation of pharmaceutically acceptable salts.

Furthermore, compounds of the present invention may exist in amorphous form and/or one or more crystalline forms, and as such all amorphous and crystalline forms and mixtures thereof of the compounds of Formula I are intended to be included within the scope of the present invention. In addition, some of the compounds of the instant invention may form solvates with water (i.e., a hydrate) or common organic solvents. Such solvates and hydrates, particularly the pharmaceutically acceptable solvates and hydrates, of the compounds of of this invention are likewise encompassed within the scope of the compounds defined by Formula I and the pharmaceutically acceptable salts thereof, along with un-solvated and anhydrous forms of such compounds.

The instant invention encompasses any composition comprised of a compound of Formula I or a compound that is a salt thereof, including for example but not limited to, a composition comprised of said compound associated together with one or more additional molecular and/or ionic component(s) which may be referred to as a “co-crystal.” The term “co-crystal” as used herein refers to a solid phase (which may or may not be crystalline) wherein two or more different molecular and/or ionic components (generally in a stoichiometric ratio) are held together by non-ionic interactions including but not limited to hydrogen-bonding, dipole-dipole interactions, dipole-quadrupole interactions or dispersion forces (van der Waals). There is no proton transfer between the dissimilar components and the solid phase is neither a simple salt nor a solvate. A discussion of co-crystals can be found, e.g., in S. Aitipamula et al., Crystal Growth and Design, 2012, 12 (5), pp. 2147-2152.

More specifically with reference to this invention, a co-crystal is comprised of a compound of Formula I or a pharmaceutically acceptable salt thereof, and one or more non-pharmaceutically active component(s) which is not biologically or otherwise undesirable (e.g., is neither toxic nor otherwise deleterious to the recipient thereof). Co-crystals can be obtained from a compound of Formula I, or a pharmaceutically acceptable salt thereof, by customary methods known in the chemical arts. For example, co-crystals comprised of a compound of this invention could be prepared by adding an acid or a neutral molecule at the desired stoichiometry to the compound, adding an appropriate solvent to achieve dissolution and, for example, precipitating, lyophilizing or concentrating the solution to obtain the solid composition. The co-crystal can be, but is not limited to, an embodiment wherein the composition is comprised of a neutral compound (i.e. not a salt form) of Formula I and one or more non-pharmaceutically active component(s); and in a further embodiment, the co-crystal composition is crystalline. Crystalline compositions may be prepared, for example, by adding an acid or a neutral molecule at the desired stoichiometry to the compound of Formula I, adding an appropriate solvent and heating to achieve complete dissolution, and then allowing the solution to cool and the crystals to grow. The present invention also includes all co-crystals of the compounds of this invention which, owing to low physiological compatibility, are not directly suitable for use in pharmaceuticals but which can be used, for example, as intermediates for chemical reactions or for the preparation of pharmaceutically acceptable co-crystals or salts.

Accordingly, the compounds of Formula I, embodiments thereof and specific compounds described and claimed herein encompass all possible pharmaceutically acceptable salts, stereoisomers, tautomers, physical forms (e.g., amorphous and crystalline forms), co-crystal compositions, solvate and hydrate forms and any combination of the foregoing forms where such forms are possible.

The compounds of Formula I described herein are prodrugs. A discussion of prodrugs is provided in (a) Stella, V. J.; Borchardt, R. T.; Hageman, M. J.; Oliyai, R.; Maag, H. et al. Prodrugs: Challenges and Rewards Part 1 and Part 2; Springer, p. 726: New York, N.Y., USA, 2007, (b) Rautio, J.; Kumpulainen, H.; Heimbach, T.; Oliyai, R.; Oh, D. et al. Prodrugs: design and clinical applications. Nat. Rev. Drug Discov. 2008, 7, 255, (c) T. Higuchi and V. Stella, Pro-drugs as Novel Delivery Systems (1987) 14 of the A.C.S. Symposium Series, and in (d) Bioreversible Carriers in Drug Design, (1987) Edward B. Roche, ed., American Pharmaceutical Association and Pergamon Press. More specifically, compounds of Formula I (or any embodiment thereof and pharmaceutically acceptable salts thereof) are prodrug modifications of tenofovir, which is a mono-phosphonate. The compounds of Formula I may be converted intracellularly (in vivo or in vitro) to the corresponding monophosphate or diphosphate of tenofovir. The conversion may occur by one or more mechanisms, e.g., an enzyme-catalyzed chemical reaction, a metabolic chemical reaction, and/or a spontaneous chemical reaction (e.g., solvolysis), such as, for example, through hydrolysis in blood. While not wishing to be bound by any particular theory, tenofovir diphosphate is generally understood to be responsible for inhibiting the HIV RT enzyme and for the resulting antiviral activity after administration of the compound of Formula I to a subject.

Another embodiment of the present invention is a compound of Formula I wherein the compound or its salt is in a substantially pure form. As used herein “substantially pure” means suitably at least about 60 wt. %, typically at least about 70 wt. %, preferably at least about 80 wt. %, more preferably at least about 90 wt. % (e.g., from about 90 wt. % to about 99 wt. %), even more preferably at least about 95 wt. % (e.g., from about 95 wt. % to about 99 wt. %, or from about 98 wt. % to 100 wt. %), and most preferably at least about 99 wt. % (e.g., 100 wt. %) of a product containing a compound of Formula I or its salt (e.g., the product isolated from a reaction mixture affording the compound or salt) consists of the compound or salt. The level of purity of the compounds and salts can be determined using a standard method of analysis such as, high performance liquid chromatography, and/or mass spectrometry or NMR techniques. If more than one method of analysis is employed and the methods provide experimentally significant differences in the level of purity determined, then the method providing the highest purity level governs. A compound or salt of 100% purity is one which is free of detectable impurities as determined by a standard method of analysis. With respect to a compound of the invention which has one or more asymmetric centers and can occur as mixtures of stereoisomers, a substantially pure compound can be either a substantially pure mixture of the stereoisomers or a substantially pure individual stereoisomer.

The compounds of Formula I herein, and pharmaceutically acceptable salts thereof, are useful for HIV reverse transcriptase inhibition and for inhibiting HIV replication in vitro and in vivo. More particularly, the compounds of Formula I for inhibiting the polymerase function of HIV-1 reverse transcriptase. The testing of compounds of the Examples of this invention in the Viking assay set forth in Example 29 below, illustrate the ability of compounds of the invention to inhibit the RNA-dependent DNA polymerase activity of HIV-1 reverse transcriptase. The compounds of Formula I may also be useful agents against HIV-2. The compounds of Examples 1-28 (inclusive of A and B isomers) of the present invention also exhibit activity against drug resistant forms of HIV (e.g., NNRTI-associated mutant strains K103N and/or Y181C; NRTI-associated mutant strains M184V and M184I mutants). This invention also encompasses methods for the treatment or prophylaxis of infection by HIV, for the inhibition of HIV reverse transcriptase, for the treatment, prophylaxis, or delay in the onset of AIDS in a subject in need thereof, which comprise administering to the subject an effective amount of a compound of the invention or a pharmaceutically acceptable salt thereof.

The invention further encompasses methods for the treatment or prophylaxis of infection by HIV, for the inhibition of HIV reverse transcriptase, for the treatment, prophylaxis, or delay in the onset of AIDS in a subject in need thereof, which comprise administering to the subject an effective amount of a compound of the invention or a pharmaceutically acceptable salt thereof in combination with an effective amount of one or more additional anti-HIV agents selected from the group consisting of HIV antiviral agents, immunomodulators, and anti-infective agents. Within this embodiment, the anti-HIV agent is an antiviral selected from the group consisting of HIV protease inhibitors, HIV reverse transcriptase inhibitors, HIV integrase inhibitors, HIV fusion inhibitors, HIV entry inhibitors, and HIV maturation inhibitors.

The invention encompasses a pharmaceutical composition comprising an effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier. The invention also encompasses a pharmaceutical composition comprising an effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier further comprising an effective amount of one or more additional anti-HIV agents selected from the group consisting of HIV antiviral agents, immunomodulators, and anti-infective agents. Within this embodiment, the anti-HIV agent is an antiviral selected from the group consisting of HIV protease inhibitors, HIV reverse transcriptase inhibitors, HIV integrase inhibitors, HIV fusion inhibitors, HIV entry inhibitors, and HIV maturation inhibitors.

The compounds of this invention could also be useful for inhibition of HBV reverse transcriptase. Accordingly, this invention also encompasses methods for the treatment of chronic hepatitis B which comprise administering to the subject an effective amount of a compound of the invention or a pharmaceutically acceptable salt thereof.

The invention also encompasses a compound of the invention, or a pharmaceutically acceptable salt thereof, for use in the preparation of a medicament for the treatment or prophylaxis of infection by HIV, for the inhibition of HIV reverse transcriptase, or for the treatment, prophylaxis, or delay in the onset of AIDS in a subject in need thereof.

Other embodiments of the present invention include the following:

-   -   (a) A pharmaceutical composition comprising an effective amount         of a compound of Formula I or a pharmaceutically acceptable salt         thereof, and a pharmaceutically acceptable carrier.     -   (b) A pharmaceutical composition which comprises the product         prepared by combining (e.g., mixing) an effective amount of a         compound of Formula I or a pharmaceutically acceptable salt         thereof, and a pharmaceutically acceptable carrier.     -   (c) The pharmaceutical composition of (a) or (b), further         comprising an effective amount of one or more an anti-HIV agents         selected from the group consisting of HIV antiviral agents,         immunomodulators, and anti-infective agents.     -   (d) The pharmaceutical composition of (c), wherein the anti-HIV         agent is selected from one or more of an antiviral selected from         the group consisting of HIV protease inhibitors, nucleoside HIV         reverse transcriptase inhibitors, non-nucleoside HIV reverse         transcriptase inhibitors, HIV integrase inhibitors, HIV fusion         inhibitors, HIV entry inhibitors and HIV maturation inhibitors.     -   (e) A combination which is (i) a compound of Formula I or a         pharmaceutically acceptable salt thereof and (ii) an anti-HIV         agent selected from the group consisting of HIV antiviral         agents, immunomodulators, and anti-infective agents; wherein the         compound and the anti-HIV agent are each employed in an amount         that renders the combination effective for inhibition of HIV         reverse transcriptase, for treatment or prophylaxis of infection         by HIV, or for treatment, prophylaxis of, or delay in the onset         or progression of AIDS.     -   (f) The combination of (e), wherein the anti-HIV agent is an         antiviral selected from the group consisting of HIV protease         inhibitors, nucleoside HIV reverse transcriptase inhibitors,         non-nucleoside HIV reverse transcriptase inhibitors, HIV         integrase inhibitors, HIV fusion inhibitors, HIV entry         inhibitors and HIV maturation inhibitors.     -   (g) A method for the inhibition of HIV reverse transcriptase in         a subject in need thereof which comprises administering to the         subject an effective amount of a compound of Formula I or         pharmaceutically acceptable salt thereof     -   (h) A method for the prophylaxis or treatment of infection by         HIV (e.g., HIV-1) in a subject in need thereof which comprises         administering to the subject an effective amount of a compound         of Formula I or pharmaceutically acceptable salt thereof     -   (i) The method of (h), wherein the compound of Formula I or a         pharmaceutically acceptable salt thereof is administered in         combination with an effective amount of at least one other HIV         antiviral selected from the group consisting of HIV protease         inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse         transcriptase inhibitors, nucleoside HIV reverse transcriptase         inhibitors, HIV fusion inhibitors, HIV entry inhibitors and HIV         maturation inhibitors.     -   (j) A method for the prophylaxis, treatment or delay in the         onset or progression of AIDS in a subject in need thereof which         comprises administering to the subject an effective amount of a         compound of Formula I or pharmaceutically acceptable salt         thereof.     -   (k) The method of (j), wherein the compound is administered in         combination with an effective amount of at least one other HIV         antiviral selected from the group consisting of HIV protease         inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse         transcriptase inhibitors, nucleoside HIV reverse transcriptase         inhibitors, HIV fusion inhibitors, HIV entry inhibitors and HIV         maturation inhibitors.     -   (l) A method for the inhibition of HIV reverse transcriptase in         a subject in need thereof which comprises administering to the         subject the pharmaceutical composition of (a), (b), (c) or (d)         or the combination of (e) or (f).

(m) A method for the prophylaxis or treatment of infection by HIV (e.g., HIV-1) in a subject in need thereof, which comprises administering to the subject the pharmaceutical composition of (a), (b), (c) or (d) or the combination of (e) or (f).

(n) A method for the prophylaxis, treatment, or delay in the onset or progression of AIDS in a subject in need thereof which comprises administering to the subject the pharmaceutical composition of (a), (b), (c) or (d) or the combination of (e) or (f).

The present invention also includes a compound of Formula I or pharmaceutically acceptable salt thereof (i) for use in, (ii) for use as a medicament for, or (iii) for use in the preparation of a medicament for: (a) therapy (e.g., of the human body), (b) medicine, (c) inhibition of HIV reverse transcriptase, (d) treatment or prophylaxis of infection by HIV, or (e) treatment, prophylaxis of, or delay in the onset or progression of AIDS. In these uses, the compounds of the present invention can optionally be employed in combination with one or more anti-HIV agents selected from HIV antiviral agents, anti-infective agents, and immunomodulators.

Additional embodiments of the invention include the pharmaceutical compositions, combinations and methods set forth in (a)-(n) above and the uses (i)(a)-(e) through (iii)(a)-(e) set forth in the preceding paragraph, wherein the compound of the present invention employed therein is a compound of one of the embodiments, aspects, classes, sub-classes, or features described above. In all of these embodiments etc., the compound may optionally be used in the form of a pharmaceutically acceptable salt.

Additional embodiments of the present invention include each of the pharmaceutical compositions, combinations, methods and uses set forth in the preceding paragraphs, wherein the compound of the present invention or its salt employed therein is substantially pure. With respect to a pharmaceutical composition comprising a compound of Formula I or its salt and a pharmaceutically acceptable carrier and optionally one or more excipients, it is understood that the term “substantially pure” is in reference to a compound of Formula I or its salt per se.

Still additional embodiments of the present invention include the pharmaceutical compositions, combinations and methods set forth in (a)-(n) above and the uses (i)(a)-(e) through (iii)(a)-(e) set forth above, wherein the HIV of interest is HIV-1. Thus, for example, in the pharmaceutical composition (d), the compound of Formula I is employed in an amount effective against HIV-1 and the anti-HIV agent is an HIV-1 antiviral selected from the group consisting of HIV-1 protease inhibitors, HIV-1 reverse transcriptase inhibitors, HIV-1 integrase inhibitors, HIV-1 fusion inhibitors, HIV-1 entry inhibitors and HIV-1 maturation inhibitors. The compounds of Formula I may also be useful agents against HIV-2.

The term “administration” and variants thereof (e.g., “administering” a compound) in reference to a compound of Formula I means providing the compound to the individual in need of treatment or prophylaxis and includes both self-administration and administration to the patient by another person. When a compound is provided in combination with one or more other active agents (e.g., antiviral agents useful for treating or prophylaxis of HIV infection or AIDS), “administration” and its variants are each understood to include provision of the compound and other agents at the same time or at different times. When the agents of a combination are administered at the same time, they can be administered together in a single composition or they can be administered separately.

As used herein, the term “composition” is intended to encompass a product comprising the specified ingredients, as well as any product which results from combining the specified ingredients. Ingredients suitable for inclusion in a pharmaceutical composition are pharmaceutically acceptable ingredients, which means the ingredients must be compatible with each other and not deleterious to the recipient thereof.

The term “subject” or “patient” as used herein refers to an animal, preferably a mammal, most preferably a human, who has been the object of treatment, observation or experiment.

The term “effective amount” as used herein means an amount of a compound sufficient to inhibit HIV reverse transcriptase, inhibit HIV replication, exert a prophylactic effect, and/or a exert a therapeutic effect after administration. One embodiment of “effective amount” is a “therapeutically effective amount” which is an amount of a compound that is effective for inhibiting HIV reverse transcriptase, inhibiting HIV replication (either of the foregoing which may also be referred to herein as an “inhibition effective amount”), treating HIV infection, treating AIDS, delaying the onset of AIDS, and/or slowing progression of ARC or AIDS in a patient infected with HIV. Another embodiment of “effective amount” is a “prophylactically effective amount” which is an amount of the compound that is effective for prophylaxis of HIV infection in a subject not infected with HIV, or prophylaxis of ARC or AIDS in an HIV-infected patient. It is understood that an effective amount can simultaneously be both a therapeutically effective amount, e.g., for treatment of HIV infection, and a prophylactically effective amount, e.g., for prevention or reduction of risk for developing AIDS. The term “preventing,” as used herein with respect to an HIV viral infection or AIDS, refers to reducing the likelihood or severity of HIV infection or AIDS.

In the combination therapies of the present invention, an effective amount can refer to each individual agent or to the combination as a whole, wherein the amounts of all agents administered in the combination are together effective, but wherein a component agent of the combination may or may not be present individually in an effective amount with reference to what is considered effective for that component agent if it were were administered alone.

In the method of the present invention (i.e., inhibiting HIV reverse transcriptase, treating or prophylaxis of HIV infection, inhibiting HIV replication, treating or prophylaxis of AIDS, delaying the onset of AIDS, or delaying or slowing progression of AIDS), the compounds of this invention, optionally in the form of a salt, can be administered by means that produce contact of the active agent with the agent's site of action. They can be administered by conventional means available for use in conjunction with pharmaceuticals, either as individual therapeutic agents or in a combination of therapeutic agents. They can be administered alone, but typically are administered with a pharmaceutical carrier selected on the basis of the chosen route of administration and standard pharmaceutical practice. The compounds of the invention can, for example, be administered orally (e.g., via tablet or capsule), parenterally (including subcutaneous injections, intravenous, intramuscular or intrasternal injection, or infusion techniques), by inhalation spray, or rectally, in the form of a unit dosage of a pharmaceutical composition containing an effective amount of the compound and conventional non-toxic pharmaceutically acceptable carriers, adjuvants and vehicles. The compound could also be administered via an implantable drug delivery device adapted to provide an effective amount of the compound or a pharmaceutical composition of the compound over an extended period of time.

Solid preparations suitable for oral administration (e.g., powders, pills, capsules and tablets) can be prepared according to techniques known in the art and can employ such solid excipients as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like. Liquid preparations suitable for oral administration (e.g., suspensions, syrups, elixirs and the like) can be prepared according to techniques known in the art and can employ any of the usual media such as water, glycols, oils, alcohols and the like. Parenteral compositions can be prepared according to techniques known in the art and typically employ sterile water as a carrier and optionally other ingredients, such as a solubility aid. Injectable solutions can be prepared according to methods known in the art wherein the carrier comprises a saline solution, a glucose solution or a solution containing a mixture of saline and glucose. Implantable compositions can be prepared according to methods known in the art wherein the carrier comprises the active chemical ingredient with polymers as suitable excipients, or utilizing an implantable device for drug delivery. Further description of methods suitable for use in preparing pharmaceutical compositions for use in the present invention and of ingredients suitable for use in said compositions is provided in Remington's Pharmaceutical Sciences, 18th edition, edited by A. R. Gennaro, Mack Publishing Co., 1990 and in Remington—The Science and Practice of Pharmacy, 22nd Edition, published by Pharmaceutical Press and Philadelphia College of Pharmacy at University of the Sciences, 2012, ISBN 978 0 85711-062-6 and prior editions.

Formulations of compounds described by Formula I that result in drug supersaturation and/or rapid dissolution may be utilized to facilitate oral drug absorption. Formulation approaches to cause drug supersaturation and/or rapid dissolution include, but are not limited to, nanoparticulate systems, amorphous systems, solid solutions, solid dispersions, and lipid systems. Such formulation approaches and techniques for preparing them are well known in the art. For example, solid dispersions can be prepared using excipients and processes as described in reviews (e.g., A. T. M. Serajuddin, J Pharm Sci, 88:10, pp. 1058-1066 (1999)). Nanoparticulate systems based on both attrition and direct synthesis have also been described in reviews such as Wu et al (F. Kesisoglou, S. Panmai, Y. Wu, Advanced Drug Delivery Reviews, 59:7 pp. 631-644 (2007)).

The compounds of Formula I can be administered in a dosage range of 0.001 to 1000 mg/kg of mammal (e.g., human) body weight per day, or at longer time intervals on non-consecutive days as appropriate, in a single dose or in divided doses. One example of a dosage range is 0.01 to 500 mg/kg body weight per day, or at other time intervals as appropriate, administered orally or via other routes of administration in a single dose or in divided doses.

Another example of a dosage range is 0.1 to 100 mg/kg body weight per day, or at other time intervals as appropriate, administered orally or via other routes of administration in single or divided doses. Another example of a dosage range is 50 mg to 1 gram per day, in a single dose or divided doses. When the compound of Formula I is administered as a salt, reference to an amount of the compound in milligrams or grams is based on the free form (i.e., the non-salt form) of the compound. Daily or weekly administration can be via any suitable route of administration but is preferably via oral administration and can be a single dose or more than one dose at staggered times (divided daily doses) within each 24 hour period, whether the dosing regimen is daily or once-weekly. Each dose may be administered using one or multiple dosage units as appropriate.

For weekly or less frequent dosing regimens with longer time intervals on non-consecutive days, a parenteral route of administration may be employed. Examples of such dosing regimens with longer time intervals on non-consecutive days include but are not limited to administration once weekly, once bi-weekly (once every two weeks with leeway as to exact date of dosing), once monthly (e.g., once every 30 days, or the same calendar day each month with leeway as to exact date of dosing), once bimonthly (e.g., once every 60 days, or the same calendar day every two months with leeway as to exact date of dosing), once every 3 months (e.g., once every 90 days, or the same calendar day every three months with leeway as to exact date of dosing), once every six months (e.g., once every 180 days, or the same calendar day every six months with leeway as to exact date of dosing), or once yearly (e.g., once every 12 months with leeway as to exact date of the annual dosing). For oral (e.g., tablets or capsules) or other routes of administration, the dosage units may contain 1.0 mg to 1000 mg of the active ingredient, for example but not limited to, 1, 5, 10, 15, 20, 25, 50, 75, 100, 150, 200, 250, 300, 350, 400, 450, 500, 600, 700, 800, 900 or 1000 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. Furthermore, the compound may be formulated in oral formulations for immediate or modified release such as extended or controlled release.

The favorable pharmacokinetic profile of tested compounds of this invention may also render the compounds suitable for less frequent dosing. Thus, the compounds of the invention could be administered orally, weekly or parenterally at longer time intervals as described above. For parenteral administration, the compositions can be administered, e.g., intravenously (IV) or intramuscularly (IM) via injection, or using other infusion techniques. One or more of such injections or infusions may be administered at each dosing time interval as needed to deliver the appropriate amount of active agent. The compound could also be administered subcutaneously using an implantable device. For parenteral administration including implantable devices employing longer duration dosing intervals such as once monthly, once every 3 months, once every 6 months, once yearly or longer intervals, the dosage amount would be adjusted upward as needed to provide effective treatment during the time intervals between administration of each dose.

The specific dose level and frequency of dosage for any particular patient may be varied and will depend upon a variety of factors including the activity of the specific compound employed, the metabolic stability and length of action of that compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the host undergoing therapy. In some cases, depending on the potency of the compound or the individual response, it may be necessary to deviate upwards or downwards from the given dose. The amount and frequency of administration will be regulated according to the judgment of the attending clinician considering such factors.

As noted above, the present invention is also directed to use of a compound of Formula I with one or more anti-HIV agents. An “anti-HIV agent” is any agent which is directly or indirectly effective in the inhibition of HIV, the treatment or prophylaxis of HIV infection, and/or the treatment, prophylaxis or delay in the onset or progression of AIDS. It is understood that an anti-HIV agent is effective in treating, preventing, or delaying the onset or progression of HIV infection or AIDS and/or diseases or conditions arising therefrom or associated therewith. For example, the compounds of this invention may be effectively administered, whether at periods of pre-exposure and/or post-exposure, in combination with effective amounts of one or more anti-HIV agents selected from HIV antiviral agents, immunomodulators, antiinfectives, or vaccines useful for treating HIV infection or AIDS. Suitable HIV antivirals for use in combination with the compounds of the present invention include, for example, those listed in Table A as follows:

TABLE A Antiviral Agents for Treating HIV infection or AIDS Name Type abacavir, ABC, Ziagen ® nRTI abacavir + lamivudine, Epzicom ® nRTI abacavir + lamivudine + zidovudine, Trizivir ® nRTI amprenavir, Agenerase ® PI atazanavir, Reyataz ® PI AZT, zidovudine, azidothymidine, Retrovir ® nRTI capravirine nnRTI darunavir, Prezista ® PI ddC, zalcitabine, dideoxycytidine, Hivid ® nRTI ddI, didanosine, dideoxyinosine, Videx ® nRTI ddI (enteric coated), Videx EC ® nRTI delavirdine, DLV, Rescriptor ® nnRTI dolutegravir, Tivicay ® InI doravirine, MK-1439 nnRTI efavirenz, EFV, Sustiva ®, Stocrin ® nnRTI efavirenz + emtricitabine + tenofovir DF, Atripla ® nnRTI + nRTI EFdA (4′-ethynyl-2-fluoro-2′-deoxyadenosine) nRTI Elvitegravir InI emtricitabine, FTC, Emtriva ® nRTI emtricitabine + tenofovir DF, Truvada ® nRTI emvirine, Coactinon ® nnRTI enfuvirtide, Fuzeon ® FI enteric coated didanosine, Videx EC ® nRTI etravirine, TMC-125 nnRTI fosamprenavir calcium, Lexiva ® PI indinavir, Crixivan ® PI lamivudine, 3TC, Epivir ® nRTI lamivudine + zidovudine, Combivir ® nRTI lopinavir PI lopinavir + ritonavir, Kaletra ® PI maraviroc, Selzentry ® EI nelfmavir, Viracept ® PI nevirapine, NVP, Viramune ® nnRTI PPL-100 (also known as PL-462) (Ambrilia) PI raltegravir, MK-0518, Isentress ™ InI Rilpivirine nnRTI ritonavir, Norvir ® PI saquinavir, Invirase ®, Fortovase ® PI stavudine, d4T, didehydrodeoxythymidine, Zerit ® nRTI tipranavir, Aptivus ® PI vicriviroc EI EI = entry inhibitor; FI = fusion inhibitor; InI = integrase inhibitor; PI = protease inhibitor; nRTI = nucleoside reverse transcriptase inhibitor; nnRTI = non-nucleoside reverse transcriptase inhibitor. Some of the drugs listed in the table are used in a salt form; e.g., abacavir sulfate, delavirdine mesylate, indinavir sulfate, atazanavir sulfate, nelfmavir mesylate, saquinavir mesylate.

It is understood that the scope of combinations of the compounds of this invention with anti-HIV agents is not limited to the HIV antivirals listed in Table A, but includes in principle any combination with any pharmaceutical composition useful for the treatment or prophylaxis of AIDS. The HIV antiviral agents and other agents will typically be employed in these combinations in their conventional dosage ranges and regimens as reported in the art, including, for example, the dosages described in the Physicians' Desk Reference, Thomson PDR, Thomson PDR, 57th edition (2003), the 58th edition (2004), or the 59th edition (2005) and the current Physicians' Desk Reference (68th ed.). (2014), Montvale, N.J.: PDR Network. The dosage ranges for a compound of the invention in these combinations can be the same as those set forth above.

The compounds of this invention are also useful in the preparation and execution of screening assays for antiviral compounds. For example, the compounds of this invention are useful for isolating enzyme mutants, which are excellent screening tools for more powerful antiviral compounds. Furthermore, the compounds of this invention are useful in establishing or determining the binding site of other antivirals to HIV reverse transcriptase, e.g., by competitive inhibition.

Abbreviations and acronyms employed herein include the following:

Ac acetyl ACN acetonitrile AcOH or HOAc acetic acid APCI atmospheric-pressure chemical ionization aq aqueous Bn benzyl Boc or BOC tert-butoxycarbonyl Bu butyl Bz benzoyl calc'd calculated cBu cyclobutyl Cbz benyzloxycarbonyl cHex cyclohexyl cPen cyclopentyl cPr cyclopropyl DCE 1,2-dichloroethane DCM dichloromethane DIEA or Hünig's base N,N-diisopropylethylamine DMA 1,2-dimethylacetamide DMF dimethylformamide DMSO dimethyl sulfoxide EDC 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide EDTA ethylenediamine tetraacetic acid ESI electrospray ionization Et ethyl EtOH ethanol EtOAc ethyl acetate g grams h hour HATU N,N,N′,N′-tetramethyl-O-(7-azabenzo- triazol-1-yl)uronium hexafluorophosphate HOBt 1-hydroxybenzotriazole HPLC high-performance liquid chromatography IPA isopropanol iPr isopropyl LC liquid chromatography LCMS liquid chromatography mass spectrometry mCPBA m-choroperoxybenzoic acid Me methyl MeOH methanol mg milligrams min minute μL microliters mL milliliters mmol millimoles MS mass spectrometry Ms methanesulfonyl (mesyl) MTBE methyl tert-butyl ether NMR nuclear magnetic resonance spectroscopy obsv'd observed Ph phenyl Pr propyl rac racemic mixture RT or rt room temperature (ambient, about 25° C.) sat or sat'd saturated SFC supercritical fluid chromatography tBu tert-butyl TEA triethylamine (Et₃N) TFA trifluoroacetic acid THF tetrahydrofuran TLC thin layer chromatography

Several methods for preparing the compounds of this invention are described in the following Schemes and Examples. Starting materials and intermediates are purchased or are made using known procedures, or as otherwise illustrated. A frequently applied route to the compounds of Formula I are described in the Scheme that follows. In some cases the order of carrying out the reaction steps in the schemes may be varied to facilitate the reaction or to avoid unwanted reaction products.

Symmetrical compounds of Formula II can be prepared from (R)-(((1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonic acid, referred to herein as TFV, with variably-substituted beta-amino esters in a one-step one-pot condensation reaction with 2,2′-dipyridyldisulfide (Aldrithiol), triphenylphosphine, and base. Amino esters that are not commercially available can be readily prepared by condensation between the corresponding amino acid and alcohols with thionyl chloride.

Multiple procedures have been developed for the synthesis of unsymmetrial compounds of the Formula IV and Formula V. In one such example, compounds of the Formula S-III can be prepared from TFV, with L-amino esters under EDC coupling conditions. The subsequent reaction of S-III with a corresponding beta-amino ester under 2,2′-dipyridyldisulfide (Aldrithiol) condensation conditions yields the products of the Formula S-IV. Amino esters that are not commercially available can be readily prepared by condensation between the corresponding amino acid and alcohols with thionyl chloride.

Similarly, compounds of the Formula R-III can be prepared from TFV, with D-amino esters under EDC coupling conditions. The subsequent reaction of R-III with a corresponding beta-amino ester under 2,2′-dipyridyldisulfide (Aldrithiol) condensation conditions yields the products of the Formula R-IV. Amino esters that are not commercially available can be readily prepared by condensation between the corresponding amino acid and alcohols with thionyl chloride.

Finally, unsymmetrical compounds of the Formula V can be prepared in a two-step one-pot procedure. In this caseTFV is initially condensed with geminally di-substituted unnatural amino esters in the first step with 2,2′-dipyridyldisulfide (Aldrithiol), triphenylphosphine, and base. Next, variably substituted beta-amino esters are added to the one-pot reaction to furnish the products of the Formula V. Amino esters that are not commercially available can be readily prepared by condensation between the corresponding amino acid and alcohols with thionyl chloride.

Reactions sensitive to moisture or air were performed under nitrogen or argon using anhydrous solvents and reagents. The progress of reactions was determined by either analytical thin layer chromatography (TLC) usually performed with E. Merck pre-coated TLC plates, silica gel 60E-254, layer thickness 0.25 mm or liquid chromatography-mass spectrometry (LC-MS).

Typically the analytical LC-MS system used consisted of a Waters ZQ™ platform with electrospray ionization in positive ion detection mode with an Agilent 1100 series HPLC with autosampler. The column was commonly a Waters Xterra MS C18, 3.0×50 mm, 5 μm or a Waters Acquity UPLC® BEH C18 1.0×50 mm, 1.7 μm. The flow rate was 1 mL/min, and the injection volume was 10 μL. UV detection was in the range 210-400 nm. The mobile phase consisted of solvent A (water plus 0.05% TFA) and solvent B (acetonitrile plus 0.05% TFA) with a gradient of 100% solvent A for 0.7 min changing to 100% solvent B over 3.75 min, maintained for 1.1 min, then reverting to 100% solvent A over 0.2 min.

Preparative HPLC purifications were usually performed using either a mass spectrometry directed system or a non-mass guided system. Usually they were performed on a Waters Chromatography Workstation configured with LC-MS System consisting of: Waters ZQ™ single quad MS system with Electrospray Ionization, Waters 2525 Gradient Pump, Waters 2767 Injecto/Collector, Waters 996 PDA Detector, the MS Conditions of: 150-750 amu, Positive Electrospray, Collection Triggered by MS, and a Waters SUNFIRE® C-18 5 micron, 30 mm (id)×100 mm column. The mobile phases consisted of mixtures of acetonitrile (10-100%) in water containing 0.1% TFA. Flow rates were maintained at 50 mL/min, the injection volume was 1800 μL, and the UV detection range was 210-400 nm. An alternate preparative HPLC system used was a Gilson Workstation consisting of: Gilson GX-281 Injector/Collector, Gilson UV/VIS-155 Detector, Gilson 333 and 334 Pumps, and either a Phenomenex Gemini-NX C-18 5 micron, 50 mm (id)×250 mm column or a Waters XBridge™ C-18 5 micron OBD™, 30 mm (id)×250 mm column. The mobile phases consisted of mixtures of acetonitrile (0-75%) in water containing 5 mmol (NH₄)HCO₃. Flow rates were maintained at 50 mL/min for the Waters Xbridge™ column and 90 mL/min for the Phenomenex Gemini column. The injection volume to ranged from 1000-8000 μL, and the UV detection range was 210-400 nm. Mobile phase gradients were optimized for the individual compounds. Reactions performed using microwave irradiation were normally carried out using an Emrys Optimizer manufactured by Personal Chemistry, or an Initiator manufactured by Biotage. Concentration of solutions was carried out on a rotary evaporator under reduced pressure. Flash chromatography was usually performed using either a Biotage® Flash Chromatography apparatus (Dyax Corp.), an ISCO CombiFlash® Rf apparatus, or an ISCO CombiFlash® Companion XL on silica gel (32-63 μM, 60

pore size) in pre-packed cartridges of the size noted. ¹H NMR spectra were acquired at 500 MHz spectrometers in CDCl₃ solutions unless otherwise noted. Chemical shifts were reported in parts per million (ppm). Tetramethylsilane (TMS) was used as internal reference in CD₃Cl solutions, and residual CH₃OH peak or TMS was used as internal reference in CD₃OD solutions. Coupling constants (J) were reported in hertz (Hz). Chiral analytical chromatography was most commonly performed on one of CHIRALPAK® AS, CHIRALPAK®AD, CHIRALCEL® OD, CHIRALCEL® IA, or CHIRALCEL® OJ columns (250×4.6 mm) (Daicel Chemical Industries, Ltd.) with noted percentage of either ethanol in hexane (% Et/Hex) or isopropanol in heptane (% IPA/Hep) as isocratic solvent systems. Chiral preparative chromatography was conducted on one of of CHIRALPAK AS, of CHIRALPAK AD, CHIRALCEL® OD, CHIRALCEL®IA, CHIRALCEL® OJ columns (20×250 mm) (Daicel Chemical Industries, Ltd.) with desired isocratic solvent systems identified on chiral analytical chromatography or by supercritical fluid (SFC) conditions.

Unless specified otherwise, it is understood that each chiral center in a compound may exist in the “S” or “R” stereoconfiguration, or as a mixture of both. Some compounds of Formula I may contain a phosphorus chiral center. Examples 6-28 contain a phosphorus chiral center. The isomer mixture in each of Examples 6-28, was separated providing an Isomer #A, e.g., Isomer 6A (faster eluting isomer) and an Isomer #B, e.g., Isomer 6B (slower eluting isomer), based on their observed elution order resulting from the separation as performed in the Example. Retention times are provided only to show the relative order of elution of each isomer in an Example. Elution order of separated isomers may differ if performed under conditions different than those employed herein. Absolute stereochemistry (R or S) of the phosphorus chiral center in each of the “A” and “B” separated stereoisomers in Examples 6-23 and 26-28 was not determined and “A” and “B” only refer to elution order. Absolute stereochemistry (R or S) of the phosphorus chiral center was determined for each of the “A” and “B” separated isomers in Examples 24 and 25. An asterisk (*) may be used in the associated chemical structure drawings of the Example compounds to indicate the phosphorus chiral center.

Intermediate A

(R)-isopropyl 3-aminobutanoate hydrochloride

Thionyl chloride (6.9 g, 58.2 mmol) was added dropwise to a solution of (R)-3-aminobutanoic acid (2 g, 19.4 mmol) in propan-2-ol (30 mL) at −50° C. The mixture was allowed to warm to ambient temperature, and then heated at 80° C. for 6 hours. The reaction mixture was concentrated under reduced pressure to give a residue, which was triturated with ice-cold diethyl ether to provide the title compound: LC/MS: [(M+1)]⁺=146.1.

Intermediate B

(R)-cyclopentyl 2-aminopropanoate

INTERMEDIATE B was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (7.8 g, 67.3 mmol) and (R)-2-aminopropanoic acid (2.0 g, 22.5 mmol) in cyclopentanol (60 mL): LC/MS: [(M+1)]⁺=158.1.

Intermediate C

(S)-isopropyl 3-amino-2-methylpropanoate hydrochloride

INTERMEDIATE C was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (6.9 g, 58.2 mmol) and (S)-3-aminobutanoic acid (2 g, 19.4 mmol) in propan-2-ol (30 mL): LC/MS: [(M+1)]⁺=146.2

Intermediate D

(R)-isopropyl 3-amino-2-methylpropanoate hydrochloride

INTERMEDIATE D was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (3.4 g, 29.1 mmol) and (R)-3-amino-2-methylpropanoic acid (1 g, 9.7 mmol) in propan-2-ol (30 mL): LC/MS: [(M+1)]⁺=146.1.

Intermediate E

(S)-isopropyl 3-amino-2-methylpropanoate hydrochloride

INTERMEDIATE E was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (3.4 g, 29.1 mmol) and (S)-3-amino-2-methylpropanoic acid (1 g, 9.7 mmol) in propan-2-ol (30 mL): LC/MS: [(M+1)]⁺=146.0.

Intermediate F

isopropyl (s)-3-amino-4-methylpentanoate hydrochloride

INTERMEDIATE F was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (8.16 g, 68.6 mmol) and (S)-3-amino-4-methylpentanoic acid (3 g, 22.87 mmol) in propan-2-ol (50 mL): LC/MS: [(M+1)]⁺=174.0.

Intermediate G

(S)-cyclopentyl 2-aminopropanoate

INTERMEDIATE G was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (7.8 g, 67.3 mmol) and (S)-2-aminopropanoic acid (2.0 g, 22.5 mmol) in cyclopentanol (60 mL): LC/MS: [(M+1)]⁺=158.0

Intermediate H

(S)-cyclobutyl 2-aminopropanoate hydrochloride

INTERMEDIATE H was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (7.8 g, 67.3 mmol) and (S)-2-aminopropanoic acid (2.0 g, 22.5 mmol) in cyclobutanol (30 mL): LC/MS: [(M+1)]⁺=144.2.

Intermediate I

(S)-cyclohexyl 2-aminopropanoate hydrochloride

INTERMEDIATE I was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (8.0 g, 67.3 mmol) and (S)-2-aminopropanoic acid (2 g, 22.5 mmol) in cyclohexanol (50 mL): LC/MS: [(M+1)]⁺=172.1.

Intermediate J

(S)-isobutyl 2-aminopropanoate hydrochloride

INTERMEDIATE J was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (8.0 g, 67.3 mmol) and (S)-2-aminopropanoic acid (2 g, 22.5 mmol) in 2-methylpropan-1-ol (50 mL): LC/MS: [(M+1)]⁺=146.2.

Intermediate K

(S)-butyl 2-aminopropanoate hydrochloride

INTERMEDIATE K was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (8.0 g, 67.3 mmol) and (S)-2-aminopropanoic acid (2 g, 22.5 mmol) in butan-1-ol (50 mL): LC/MS: [(M+1)]⁺=146.2.

Intermediate L

(S)-pentyl 2-aminopropanoate hydrochloride

INTERMEDIATE L was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (8.0 g, 67.3 mmol) and (S)-2-aminopropanoic acid (2 g, 22.5 mmol) in pentan-1-ol (50 mL): LC/MS: [(M+1)]⁺=160.2.

Intermediate M

(S)-heptyl 2-aminopropanoate hydrochloride

INTERMEDIATE M was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (8.0 g, 67.3 mmol) and (S)-2-aminopropanoic acid (2 g, 22.5 mmol) in heptan-1-ol (50 mL): LC/MS: [(M+1)]⁺=188.2.

Intermediate N

(R)-cyclobutyl 2-aminopropanoate hydrochloride

INTERMEDIATE N was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (7.8 g, 67.3 mmol) and (R)-2-aminopropanoic acid (2.0 g, 22.5 mmol) in cyclobutanol (30 mL): LC/MS: [(M+1)]⁺=144.0.

Intermediate O

(R)-cyclohexyl 2-aminopropanoate hydrochloride

INTERMEDIATE 0 was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE A starting from thionyl chloride (8.0 g, 67.3 mmol) and (R)-2-aminopropanoic acid (2 g, 22.5 mmol) in cyclohexanol (50 mL): LC/MS: [(M+1)]⁺=172.1.

Intermediate P

isopropyl 2-amino-2-methylpropanoate hydrochloride

A neat solution of isopropanol (89 ml, 1164 mmol) was treated slowly with thionyl chloride (15.57 ml, 213 mmol) at room temperature over a 2 min period. (exotherm to 60° C.) The mixture was treated with 2-amino-2-methylpropanoic acid (20 g, 194 mmol) and fitted with a reflux condenser. This suspension was heated to 85° C. (reflux) and stirred for 3 days. The resulting clear solution was concentrated to dryness. The resulting oil was crystallized by tritutation in diethyl ether and hexanes. The solids were isolated by filtration and dried under high vacuum to provide the title compound: LC/MS: [(M+1)]⁺=146.1.

Intermediate Q

butyl 2-amino-2-methylpropanoate hydrochloride

INTERMEDIATE Q was prepared on 8 mmol scale in a similar fashion to that described for the synthesis of INTERMEDIATE P starting from 2-amino-2-methylpropanoic acid, except using n-butanol to provide the title compound: LC/MS: [(M+1)]⁺=160.1.

Intermediate R

pentyl 2-amino-2-methylpropanoate hydrochloride

A neat solution of pentan-1-ol (205 g, 2327 mmol) was treated slowly with thionyl chloride (15.57 ml, 213 mmol) at room temperature over a 10 min period. The mixture was treated with 2-amino-2-methylpropanoic acid (40 g, 388 mmol) and fitted with a reflux condenser and stirred at 80° C. over the weekend. The reaction mixture was concentrated under reduced pressure and then dissolved in water (1 L) and washed with 1:1 EtOAc/hexane (2×2 L), hexanes (1×2 L) and dichloromethane (3×1 L). The aqueous layer was concentrated and azeotroped with acetonitrile and then toluene. The residue was dried overnight under high vacuum. The solids were triturated with 500 mL of diethyl ether, filtered and dried to afford the title compound: LC/MS: [(M+1)]⁺=174.2.

Intermediate S

hexyl 2-amino-2-methylpropanoate hydrochloride

INTERMEDIATE S was prepared on 388 mmol scale in a similar fashion to that described for 113 the synthesis of INTERMEDIATE R starting from 2-amino-2-methylpropanoic acid, except using n-hexanol to provide the title compound: LC/MS: [(M+1)]⁺=187.9.

Intermediate T

isobutyl 2-amino-2-methylpropanoate hydrochloride

INTERMEDIATE T was prepared on 36.8 mmol scale in a similar fashion to that described for the synthesis of INTERMEDIATE R starting from from 2-amino-2-methylpropanoic acid, except using isobutanol to provide the title compound: LC/MS: [(M+1)]⁺=160.1.

Intermediate U

P-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}-N-[(1S)-1-methyl-2-(1-methylethoxy)-2-oxoethyl]phosphonamidic acid

To a solution of (R)-(((1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonic acid (referred to herein as TFV, 3.0 g, 10.5 mmol) in water (50 mL) were added EDC (10.0 g, 52.2 mmol) and (S)-isopropyl 2-aminopropanoate hydrochloride (8.8 g, 52.2 mmol) at ambient temperature. The pH value of the resulting solution was adjusted to 7.2-7.6 with TEA (5.3 g, 52.2 mmol). The resulting mixture was stirred at 40° C. for 16 hours. Upon reaction completion, the reaction mixture was cooled down to ambient temperature and concentrated under reduced pressure. The residue was purified by flash chromatography under the following condition: Column: C18, 330 g, 20-35 μm, 100 Å; Mobile Phase A: Water with 5 mM NH₄HCO₃; Mobile Phase B: ACN; Gradient: 5-20% B in 25 min; Flow rate: 50 mL/min; Detector 254 nm; retention time: 18 min to afford the title compound: LC/MS: [(M+1)]⁺=401.2.

Intermediate V

P-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}-N-[(1R)-1-methyl-2-(1-methylethoxy)-2-oxoethyl]phosphonamidic acid

INTERMEDIATE V was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with (R)-isopropyl 2-aminopropanoate hydrochloride: LC/MS: [(M+1)]⁺=401.2.

Intermediate W

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((S)-1-isobutoxy-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE W was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE J: LC/MS: [(M+1)]⁺=415.0.

Intermediate X

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((S)-3-isopropoxy-2-methyl-3-oxopropyl)phosphonamidic acid

INTERMEDIATE X was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE E: LC/MS: [(M+1)]⁺=415.1.

Intermediate Y

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((S)-1-cyclobutoxy-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE Y was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE H: LC/MS: [(M+1)]⁺=413.0.

Intermediate Z

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((S)-1-(cyclohexyloxy)-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE Z was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE I: LC/MS: [(M+1)]⁺=441.1.

Intermediate AA

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((S)-1-butoxy-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE AA was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE K: LC/MS: [(M+1)]⁺=415.0

Intermediate BB

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((S)-1-oxo-1-(pentyloxy)propan-2-yl)phosphonamidic acid

INTERMEDIATE BB was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE L: LC/MS: [(M+1)]⁺=457.2

Intermediate CC

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((S)-1-(heptyloxy)-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE CC was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE M: LC/MS: [(M+1)]⁺=429.0

Intermediate DD

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((R)-1-cyclobutoxy-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE DD was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE N: LC/MS: [(M+1)]⁺=412.9

Intermediate EE

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((R)-1-(cyclohexyloxy)-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE EE was prepared in a similar fashion to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE O: LC/MS: [(M+1)]⁺=441.1

Intermediate FF

P—(((R)-1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)-N—((R)-1-(cyclopentyloxy)-1-oxopropan-2-yl)phosphonamidic acid

INTERMEDIATE FF was prepared in a similar fashion in to that described for the synthesis of INTERMEDIATE U starting from TFV with INTERMEDIATE B: LC/MS: [(M+1)]⁺=427.0

Intermediate HH

(R)-(((1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonic dichloride hydrochloride (HH)

To a stirred suspension of (R)-(((1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonic acid hydrochloride (30 g, 93 mmol) in acetonitrile (600 mL) was added thionyl chloride (27.1 mL, 371 mmol) and the mixture was heated to 75° C. for 8 h. The mixture was cooled to room temperature and attached to a distillation apparatus. The reaction mixture was then heated to 40° C. under vacuum to carry out distillation. Distillation continued until the volume of the reaction mixture reached 150 mL. The resulting slurry was stirred at room temperature overnight. The flask was transferred to a glove box and the solid was filtered. The solid was washed with 2-MeTHF (100 mL). The solid was then dried under vacuum in the glove box to provide INTERMEDIATE HH as a solid.

For characterization by ³¹P NMR, INTERMEDIATE HH was dissolved in anhydrous MeOH to prepare the bis-methoxy adduct of HH: ³¹P NMR (202.5 MHz; CD₃OD) δ 24.55; LCMS: [(M+1)]⁺=316.11.

Example 1

1-methylethyl 8-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}-2-methyl-4-oxo-3-oxa-7,9-diaza-8-phosphadodecan-12-oate 8-oxide (1) Step 1: isopropyl 3-aminopropanoate hydrochloride (INTERMEDIATE GG)

Thionyl chloride (2.0 g, 16.8 mmol) was added dropwise to a solution of 3-aminopropanoic acid (0.5 g, 5.61 mmol) in propan-2-ol (10 mL) at 50° C. The mixture was allowed to warm to ambient temperature, and then heated at 80° C. for 6 h. The reaction mixture was concentrated under reduced pressure to provide a residue, which was triturated with ice-cold diethyl ether to provide the title compound: LC/MS: [(M+1)]⁺=132.1.

Step 2: 1-methylethyl 8-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}-2-methyl-4-oxo-3-oxa-7,9-diaza-8-phosphadodecan-12-Oate 8-Oxide

To a suspension of (R)-(((1-(6-amino-9H-purin-9-yl)propan-2-yloxy)methyl)phosphonic acid (referred to herein as TFV, 100 mg, 0.35 mmol) in pyridine (5 mL) were added INTERMEDIATE GG (183 mg, 1.39 mmol), Et₃N (211 mg, 2.09 mmol), PPh₃ (365 mg, 1.39 mmol) and 1,2-di(pyridin-2-yl)disulfane (Aldrithiol, 307 mg, 1.39 mmol) at ambient temperature. The resulting mixture was stirred at 60° C. for 16 hours under a N₂ atmosphere. The mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by gradient elution on silica gel (1% to 10% MeOH/CH₂O₂) to afford the title compound: ¹H NMR (400 MHz; CDCl₃) δ 8.37 (s, 1H), 8.03 (s, 1H), 6.04 (br s, 2H), 5.07-4.99 (m, 2H), 4.40 (dd, J=3.2; 14.4 Hz, 1H), 4.15 (dd, J=7.6; 14.4 Hz, 1H), 3.94-3.90 (m, 1H), 3.77 (dd, J=8.4; 12.8 Hz, 1H), 3.46 (dd, J=8.4; 12.8 Hz, 1H), 3.25-3.09 (m, 6H), 2.49 (t, J=6.4 Hz, 2H), 2.44 (t, J=6.4 Hz, 2H), 1.26-1.23 (m, 15H); ³¹P NMR (162 MHz; CDCl₃) δ 23.12; LC/MS: [(M+1)]⁺=514.1.

1A: Alternate Method to Prepare Compound 1

A mixture of INTERMEDIATE HH (200 mg, 0.62 mmol) and INTERMEDIATE GG (217 mg, 1.30 mmol) in 2-MeTHF (1.65 mL)/DCM (0.41 mL) was treated with trimethylamine (0.43 mL, 3.1 mmol) and stirred at room temperature for 2 h. The mixture was concentrated and the residue was dissolved in 1:1 MeCN/water (4 mL) and purified directly by reverse phase chromatography (XBridge 10 μm C18 30×250 mm column; 10-70% CH₃CN in a 5 mM solution of NH₄HCO₃ over 30 min) to afford compound 1: LC/MS: [(M+1)]⁺=514.1.

The compounds in Table 1 were prepared in an analogous fashion to that described for Example 1. The column having the heading INT provides the intermediate example compound used to make each exemplified compound.

TABLE 1 LC/MS Ex. Structure IUPAC Name (M + 1)⁺ INT. 2

1-methylethyl (6R,10R)-8-{[(1R)- 2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}-2,6,10- trimethyl-4-oxo-3-oxa-7,9-diaza- 8-phosphadodecan-12-oate 8- oxide Calc′d 542.3, found 542.1 A 3

1-methylethyl (5S,11S)-8-{[(1R)- 2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}-2,5,11- trimethyl-4-oxo-3-oxa-7,9-diaza- 8-phosphadodecan-12-oate 8- oxide Calc′d 542.3, found 542.2 E 4

1-methylethyl (5R,11R)-8-{[(1R)- 2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}-2,5,11- trimethyl-4-oxo-3-oxa-7,9-diaza- 8-phosphadodecan-12-oate 8- oxide Calc′d 542.3, found 542.1 D 5

1-methylethyl (6S,10S)-8-{[(1R)- 2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}-2,6,10- trimethyl-4-oxo-3-oxa-7,9-diaza- 8-phosphadodecan-12-oate 8- oxide Calc′d 542.3, found 542.5 C

³¹P NMR shift Ex. (ppm) Purification conditions 2 20.20 (162 MHz; silica gel column chromatography, CDCl₃) eluted with DCM:MeOH (50:1 to 10:1) 3 23.13 (162 MHz; silica gel column chromatography, CDCl₃) eluted with DCM:MeOH (50:1 to 10:1) 4 23.01 (162 MHz; silica gel column chromatography, CDCl₃) eluted with DCM:MeOH (50:1 to 10:1) 5 23.01 (162 MHz; silica gel column chromatography, CD₃OD) eluted with DCM:MeOH (50:1 to 10:1)

Examples 6A and 6B

1-methylethyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate, and 1-methylethyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate (6a and 6b)

To a solution of INTERMEDIATE U (100 mg, 0.25 mmol) in pyridine (5 mL) were added INTERMEDIATE E (43.5 mg, 0.30 mmol), Et₃N (50 mg, 0.50 mmol), 1,2-di(pyridin-2-yl)disulfane (Aldrithiol, 110 mg, 0.50 mmol) and PPh₃ (131 mg, 0.50 mmol) at ambient temperature. The resulting mixture was stirred at 60° C. for 3 hours under a N₂ atmosphere. The reaction mixture was cooled to ambient temperature and concentrated under reduced pressure. The residue was purified by gradient elution on silica gel column (1% to 10% MeOH/CH₂Cl₂) to afford a mixture of two iosmers at phosphorous. These isomers were then separated by preparative Chiral-HPLC under the following conditions: Column: Chiralpak IA 2×25 cm, 5 um; Mobile Phase: Hexane/EtOH (80/20, 25 min); Flow rate: 20 mL/min; Detector 254/220 nm to afford Isomer 6A (faster eluting, RT=14.2 min) as a solid: ¹H NMR (400 MHz; CD₃OD) δ 8.24 (s, 1H), 8.22 (s, 1H), 5.04-4.97 (m, 2H), 4.39 (dd, J=3.2 Hz, 14.4 Hz, 1H), 4.25 (q, J=7.2 Hz, 1H), 3.97-3.94 (m, 1H), 3.90-3.85 (m, 1H), 3.80 (dd, J=8.8; 13.2 Hz, 1H), 3.55 (dd, J=9.6; 13.2 Hz, 1H), 3.03-2.98 (m, 1H), 2.88-2.82 (m, 1H), 2.54-2.50 (m, 1H), 1.35 (d, J=6.8 Hz, 3H), 1.31-1.22 (m, 15H), 1.09 (d, J=6.8 Hz, 3H); ³¹P NMR (162 MHz; CD₃OD) δ 24.87; LC/MS: [(M+1)]⁺=528.5; and Isomer 6B (slower eluting, RT=20 min) as a solid: ¹H NMR (400 MHz; CD₃OD) δ 8.23 (s, 2H), 5.05-4.99 (m, 1H), 4.95-4.90 (m, 1H), 4.42 (dd, J=3.2; 14.4 Hz, 1H), 4.24 (q, J=7.2 Hz, 1H), 3.99-3.97 (m, 1H), 3.85-3.79 (m, 2H), 3.57 (dd, J=10.8; 13.2 Hz, 1H), 3.16-3.09 (m, 1H), 2.98-2.91 (m, 1H), 2.59-2.51 (m, 1H), 1.33 (d, J=7.2 Hz, 3H), 1.26-1.21 (m, 15H), 1.15 (d, J=6.8 Hz, 3H); ³¹P NMR (162 MHz; CD₃OD) δ 25.04; LC/MS: [(M+1)]⁺=528.4.

Example 7A and 7b

1-methylethyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate and 1-methylethyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate (7A and 7B)

The two title compounds were prepared in the same fashion as described for example 6A/B from INTERMEDIATE U and INTERMEDIATE AA. The two iosmers were separated by Prep-HPLC under the following conditions: Column: X Bridge C18, 19×150 mm, 5 μm; Mobile Phase A (10 mmol/L NH₄HCO₃ in water), Mobile Phase B (CH₃CN); Gradient: 25-30% B in 10 min. Flow rate: 20 mL/min; Detector: 254/220 nm; to afford Isomer 7A (faster eluting, RT=5.5 min) as a solid: ¹H NMR (400 MHz; CD₃OD) δ 8.23 (s, 1H), 8.22 (s, 1H), 5.03-4.95 (m, 2H), 4.40 (dd, J=3.2; 14.4 Hz, 1H), 4.28 (dd, J=7.2; 14.4 Hz, 1H), 3.98-3.95 (m, 1H), 3.88 (d, J=8.8 Hz, 1H), 3.79 (dd, J=7.6; 13.2 Hz, 1H), 3.56 (dd, J=9.6; 13.2 Hz, 1H), 3.10-3.05 (m, 2H), 2.43 (t, J=6.8 Hz, 2H), 1.35 (d, J=7.2 Hz, 3H), 1.28-1.21 (m, 15H); ³¹P NMR (162 MHz; CD₃OD) δ 24.93 (decoupled); LC/MS: [(M+1)]⁺=514.5; and Isomer 7B (slower eluting, RT=7.3 min) as a solid: to ¹H NMR (400 MHz; CD₃OD) δ 8.23 (s, 1H), 8.22 (s, 1H), 5.03 (q, J=6.0 Hz, 1H), 4.90 (q, J=6.0 Hz, 1H), 4.43 (dd, J=3.2; 14.4 Hz, 1H), 4.25 (dd, J=7.2; 14.8 Hz, 1H), 3.98-3.95 (m, 1H), 3.83-3.77 (m, 2H), 3.58 (dd, J=10.4; 12.8 Hz, 1H), 3.18-3.12 (m, 2H), 2.47 (t, J=6.8 Hz, 2H), 1.33 (d, J=7.2 Hz, 3H), 1.27-1.21 (m, 15H); ³¹P NMR (162 MHz; CD₃OD) δ 25.16 (decoupled); LC/MS: [(M+1)]⁺=514.5.

The compounds in Table 2 were prepared in an analogous fashion to that described for Example 6A/B. The column having the heading INT provides the intermediate example compounds used to make each exemplified compound. The diastereoisomers were separated by either Prep-HPLC or preparative Chiral-HPLC. Absolute sterochemistry of the “A” isomer (faster eluting) and “B” isomer (slower eluting) of each example was not determined.

TABLE 2 LC/MS Ex. EXAMPLE STRUCTURE/NAME (M + 1)⁺ INT. 8A and 8B

528.5 and 528.5 C and O 1-methylethyl (3S)-3-{[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2- oxoethyl]amino}phosphoryl]amino}butanoate; and 1-methylethyl (3S)-3-{[S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2- oxoethyl]amino}phosphoryl]amino}butanoate 9A and 9B

528.5 and 528.5 A and O 1-methylethyl (3R)-3-{[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2- oxoethyl]amino}phosphoryl]amino}butanoate; and 1-methylethyl (3R)-3-{[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2- oxoethyl]amino}phosphoryl]amino}butanoate 10A and 10B

528.4 and 528.5 D and O 1-methylethyl N-[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2R)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and 1-methylethyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2R)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate 11A and 11B

554.4 and 554.4 E and G cyclopentyl N-[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and cyclopentyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate 12A and 12B

540.2 and 540.2 E and Y cyclobutyl N-[(S)-{[(1R)-2-(6-amino-9-purin-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and cyclobutyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate 13A and 13B

568.5 and 568.5 E and Z cyclohexyl N-[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and cyclohexyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate 14A and 14B

542.5 and 542.4 E and W 2-methylpropyl N-[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and 2-methylpropyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate 15A and 15B

542.4 and 542.3 E and AA butyl N-[(S)-{[1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and butyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate 16A and 16B

556.5 and 556.5 E and BB pentyl N-[(S-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and pentyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate 17A and 17B

584.3 and 584.3 E and CC heptyl N-[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate; and heptyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-L-alaninate

Retention ³¹P NMR shift time Ex. (ppm) Purification conditions (min)  8A 23.25 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 13.5 CD₃OD) Mobile Phase A: Hexane; Mobile Phase  8B 23.51 (162 MHz; B: EtOH; Flow rate: 18 mL/min; 23.0 CD₃OD) Gradient: 20% B in 30 min; Detector 254 nm  9A 23.57 (162 MHz; Column: XBridge Prep C18 OBD, 1.9 * 7.5 CD₃OD) 15 cm, 5 um; Mobile Phase A: Water  9B 23.20 (162 MHz; (plus 10 mM NH₄HCO₃); Mobile Phase 8.7 CD₃OD) B: ACN; Flow rate: 20 mL/min; Gradient: 25% to 31% B in 11 min; Detector: 254 nm 10A 25.19 (162 MHz; Column: Chiralpak AD-H 2.1 * 15 cm, 5 15.0 CD₃OD) um; Mobile Phase A: Hexane; Mobile 10B 24.80 (162 MHz; Phase B: EtOH; Flow rate: 20 mL/min; 22.5 CD₃OD) Gradient: 20% B in 30 min; Detector: 254 nm 11A 24.87 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 11.3 CD₃OD) Mobile Phase A: Hexane (plus 0.1% IPA, 11B 25.05 (162 MHz; v/v); Mobile Phase B: EtOH; Flow rate: 18.6 CD₃OD) 20 mL/min; Gradient: 30% B in 25 min; Detector: 254 nm 12A 24.89 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 23.0 CD₃OD) Mobile Phase A: Hexane, Mobile Phase 12B 25.04 (162 MHz; B: EtOH; Flow rate: 20 mL/min; 38.0 CD₃OD) Gradient: 15% B in 45 min; Detector: 254 nm 13A 24.88 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 9.3 CD₃OD) Mobile Phase A: Hexane (plus 0.1% 13B 25.08 (162 MHz; DEA, v/v); Mobile Phase B: EtOH; Flow 16.4 CD₃OD) rate: 20 mL/min; Gradient: 30% B in 30 min; Detector: 254 nm 14A 24.87 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 14.0 CD₃OD) Mobile Phase A: Hexane (plus 0.1% 14B 25.05 (162 MHz; DEA, v/v); Mobile Phase B: EtOH; Flow 20.6 CD₃OD) rate: 20 mL/min; Gradient: 20% B in 30 min; Detector: 254 nm 15A 24.88 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 14.0 CD₃OD) Mobile Phase A: Hexane (plus 0.1% 15B 25.05 (162 MHz; DEA, v/v); Mobile Phase B: EtOH; 21.0 CD₃OD) Flow rate: 20 mL/min; Gradient: 20% B in 26 min; Detector: 254 nm 16A 24.87 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 11.0 CD₃OD) Mobile Phase A: Hexane (plus 0.1% 16B 25.04 (162 MHz; DEA, v/v); Mobile Phase B: EtOH; 15.4 CD₃OD) Flow rate: 20 mL/min; Gradient: 25% B in 18 min; Detector: 254 nm 17A 25.04 (162 MHz; Column: chiral pak AS-H 2 * 25 cm, 5 7.9 CD₃OD) um; Mobile Phase A: Hexane (plus 0.2% 17B 24.88 (162 MHz; IPA, v/v), Mobile Phase B: EtOH; Flow 11.5 CD₃OD) rate: 20 mL/min; Gradient: 80% to 20% B in 16.5 min; Detector: 254 nm

Example 18A and 18B

isopropyl (3R)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl) (((R)-1-cyclobutoxy-1-oxopropan-2-yl)amino)phosphoryl)amino)butanoate; and isopropyl (3R)-3-(((R)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl) (((R)-1-cyclobutoxy-1-oxopropan-2-yl)amino)phosphoryl)amino)butanoate (18A and 18B)

The two title compounds were prepared in the same way as described for example 6A/B from INTERMEDIATE DD and INTERMEDIATE A, and purified by preparative Chiral HPLC with the following condition: Column: Chiralpak IA 2×25 cm, Sum; Mobile Phase: Hexane/EtOH (85/15) in 30 min; Flow rate: 20 mL/min; Detector: 254/220 nm to afford Isomer 18A (faster eluting, RT=18.7 min) as a solid: ¹H NMR (300 MHz; CD₃OD) δ 8.18 (s, 1H), 8.16 (s, 1H), 4.97-4.91 (m, 2H), 4.34 (dd, J=3.3; 14.4 Hz, 1H), 4.23 (dd, J=6.9; 21.3 Hz, 1H), 3.95-3.91 (m, 1H), 3.91-3.82 (m, 1H), 3.79-3.72 (m, 1H), 3.65-3.58 (m, 1H), 3.53-3.48 (m, 1H), 2.43-2.25 (m, 4H), 2.12-1.97 (m, 2H), 1.81-1.75 (m, 1H), 1.63-1.57 (m, 1H), 1.35 (d, J=7.2 Hz, 3H), 1.20-1.15 (m, 9H), 1.04 (d, J=6.6 Hz, 3H); ³¹P NMR (121 MHz; CD₃OD) δ 23.37; LC/MS: [(M+1)]⁺=540.1; and Isomer 18B (slower eluting, RT=25.3 min) as a solid: ¹H NMR (300 MHz; CD₃OD) δ 8.18 (s, 1H), 8.17 (s, 1H), 4.97-4.91 (m, 2H), 4.34 (dd, J=3.3; 14.4 Hz, 1H), 4.19 (dd, J=6.9; 21.3 Hz, 1H), 3.93-3.89 (m, 1H), 3.81-3.69 (m, 2H), 3.65-3.48 (m, 2H), 2.47 (dd, J=5.7; 17.4 Hz, 1H), 2.34-2.27 (m, 3H), 2.11-1.98 (m, 2H), 1.81-1.75 (m, 1H), 1.69-1.59 (m, 1H), 1.25 (d, J=7.2 Hz, 3H), 1.19-1.13 (m, 12H); ³¹P NMR (121 MHz; CD₃OD) δ 23.289; LC/MS: [(M+1)]⁺=540.1

The compounds in Table 3 were prepared in an analogous fashion to that described for Example 18A and 18B. The column having the heading INT provides the intermediate example compounds used to make each exemplified compound. The diastereoisomers were separated by one of the four listed methods: reverse phase HPLC, chiral HPLC, SFC, or prep TLC. Absolute sterochemistry of the “A” isomer (faster eluting) and “B” isomer (slower eluting) of each example was not determined.

TABLE 3 LC/MS Ex. EXAMPLE STRUCTURE/NAME (M + 1)⁺ INT. 19A and 19B

540.1 and 540.1 C and DD 1-methylethyl (3S)-3-{[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(1R)-2-(cyclobutyloxy)-1-methyl-2- oxoethyl]amino}phosphoryl]amino}butanoate; and 1-methylethyl (3S)-3-{[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(1R)-2-(cyclobutyloxy)-1-methyl-2- oxoethyl]amino}phosphoryl]amino}butanoate 20A and 20B

540.2 and 540.2 E and DD cyclobutyl N-[(S)-{[1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate; and cyclobutyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate 21A and 21B

568.5 and 568.5 E and EE cyclohexyl N-[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate; and cyclohexyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate 22A and 22B

554.4 and 554.4 E and FF cyclopentyl N-[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate; and cyclopentyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate 23A and 23B

526.5 and 526.5 GG and DD cyclobutyl N-[(S)-{[1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate; and cyclobutyl N-[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1- methylethoxy]methyl}{[3-(1-methylethoxy)-3- oxopropyl]amino}phosphoryl]-D-alaninate

Retention ³¹P NMR shift time Ex. (ppm) Purification conditions (min) 19A 23.40 (162 MHz; Column: X Bridge C18, 1.9 * 15 cm, 5 8.6 CD₃OD) um; Mobile Phase A: Water (plus 10 mM 19B 23.24 (162 MHz; NH₄HCO₃) Mobile Phase B: ACN; Flow 10.2 CD₃OD) rate: 20 mL/min; Gradient: 10% to 90% B in 15 min; Detector: 254 nm 20A 24.83 (162 MHz; Column: Chiralpak AD-H 2 * 25 cm; 13.0 CD₃OD) Mobile Phase A: Hexane (plus 0.2% IPA, 20B 25.02 (162 MHz; v/v), Mobile Phase B: EtOH; Flow rate: 21.0 CD₃OD) 20 mL/min; Gradient: 20% B in 25 min; Detector: 254 nm 21A 24.82 (162 MHz; Column: Chiralpak IA 2 * 25 cm, 5 um; 13.0 CD₃OD) Mobile Phase A: Hexane (plus 0.2% IPA, 21B 25.03 (162 MHz; v/v); Mobile Phase B: i-PrOH; Flow rate: 20.0 CD₃OD) 20 mL/min; Gradient: 20% B in 30 min; Detector: 254 nm 22A 24.82 (162 MHz; Column: Chiralpak AD-H 2 * 25 cm, 5 10.6 CD₃OD) um; Mobile Phase A: Hexane (plus 0.2% 22B 25.04 (162 MHz; DEA, v/v); Mobile Phase B: EtOH; Flow 14.7 CD₃OD) rate: 20 mL/min; Gradient: 30% B in 16 min; Detector: 254 nm 23A 24.92 (162 MHz; Column: Chiralpak AD-H 2 * 25 cm, 5 22.3 CD₃OD) um; Mobile Phase A: Hexane (plus 0.2% 23B 25.08 (162 MHz; DEA, v/v); Mobile Phase B: EtOH; Flow 29.2 CD₃OD) rate: 20 mL/min; Gradient: 20% B in 35 min; Detector: 254 nm

Example 24A and 24B

isopropyl (3S)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate (24A); and isopropyl (3S)-3-(4R)-(4(R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate (24B)

To a mixture of TFV (5.0 g, 17.4 mmol), INTERMEDIATE R (5.5 g, 26.1 mmol) and Et₃N (14.1 g, 139 mmol) in pyridine (500 mL) were added PPh₃ (18.3 g, 69.6 mmol) and 2,2′-dipyridylsulfide (Aldrithiol, 15.3 g, 69.6 mmol). The resulting mixture was stirred for 3 hours at 60° C. under a N₂ atmosphere followed by the addition of INTERMEDIATE F (3.6 g, 17.4 mmol). After stirring for an additional 16 hours at 60° C., the resulting mixture was concentrated under reduced pressure and the residue was dissolved into EtOAc (500 mL), washed with saturated aqueous ammonium chloride (3×100 mL) and brine (100 mL), and dried over anhydrous Na₂SO₄. After filtration, the filtrate was concentrated under reduced pressure and the residue was purified by gradient elution on silica gel (1% to 10% methanol/CH₂Cl₂) to remove most of the impurities. The residue was further purified by Prep-HPLC under the following conditions: Column: X Bridge C18, 330 g, 20-35 μm, 100 Å; Mobile Phase A (5 mM NH₄HCO₃ in water), Mobile Phase B (CH₃CN); Gradient: 10 to 25% B over 15 min; then 25% to 45% B over 20 min; then 45% to 55% B over 10 min; then isocratic at 95% B for 8 min; Flow rate: 70 mL/min; Detector: 254 nm; Rt: 38 min to give provide an inseparable mixture of the title compounds. The two isomers were separated by Prep-SFC with the following condition: Column: CHIRALPAK IA, 5 cm*25 cm; Mobile Phase A: CO₂ (65%), Mobile Phase B: IPA with 0.2% isopropylamine (35%); Flow rate: 160 mL/min; Detector: 220 nm; to afford the faster eluting Isomer 24A (Rt=4.83 min): ¹H NMR (400 MHz; CD₃OD) δ 8.22 (s, 1H), 8.21 (s, 1H), 4.98-4.95 (m, 1H), 4.35 (dd, J=14.0, 2.8 Hz, 1H), 4.23 (dd, J=14.0, 6.8 Hz, 1H), 4.13-4.09 (m, 2H), 3.98-3.91 (m, 1H), 3.71 (dd, J=12.8, 8.4 Hz, 1H), 3.52-3.45 (m, 1H), 3.24-3.19 (m, 1H), 2.48-2.35 (m, 2H), 1.78-1.65 (m, 4H), 1.52-1.49 (m, 6H), 1.38-1.32 (m, 4H), 1.22-1.19 (m, 8H), 1.02 (t, J=7.6 Hz, 2H), 0.92 (t, J=6.8 Hz, 3H), 0.81-0.79 (m, 4H); ³¹P NMR (162 MHz; CD₃OD) δ 21.33; LC/MS: [(M+1)]⁺=598.4; and the slower eluting Isomer 24B (Rt=5.60 min): ¹H NMR (400 MHz; CD₃OD) δ 8.23 (s, 1H), 8.21 (s, 1H), 4.97-4.94 (m, 1H), 4.40 (dd, J=14.0, 2.8 Hz, 1H), 4.23 (dd, J=14.0, 6.8 Hz, 1H), 4.13-4.09 (m, 2H), 4.01-3.91 (m, 1H), 3.78 (dd, J=12.8, 8.4 Hz, 1H), 3.52 (dd, J=12.8, 10.0 Hz, 1H), 3.38-3.35 (m, 1H), 2.45 (dd, J=6.4, 1.6 Hz, 2H), 1.78-1.72 (m, 1H), 1.71-1.62 (m, 2H), 1.47 (s, 3H), 1.43 (s, 3H), 1.37-1.32 (m, 4H), 1.23-1.18 (m, 9H), 0.93-0.88 (m, 9H); ³¹P NMR (162 MHz; CD₃OD) δ 22.53; LC/MS: [(M+1)]⁺=598.4.

Example 25A and 25B

isopropyl (3S)-3-(4S)-(4(R)-1-(6-amino-9H-purin-9-yl)propan-2-yl(oxy)methyl)((1-isopropoxy-2-methyl-1-oxopropan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate (25A); and isopropyl (3S)-3-(4R)-(4(R)-1-(6-amino-9H-purin-9-yl)propan-2-yl(oxy)methyl)((1-isopropoxy-2-methyl-1-oxopropan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate (25B

To a suspension of (R)-(((1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphonic acid (5.0 g, 17.4 mmol) in pyridine (500 mL) were added INTERMEDIATE P (3.8 g, 20.9 mmol), Et₃N (14.1 g, 139.6 mmol), triphenylphosphine (18.3 g, 69.8 mmol) and 2,2′-dipyridylsulfide (Aldrithiol, 15.3 g, 69.8 mmol). The resulting mixture was stirred for 3 hours at 60° C. under nitrogen atmosphere followed by the addition of INTERMEDIATE F (4.1 g, 19.2 mmol). After stirring for additional 16 hours at 60° C., the resulting mixture was concentrated under reduced pressure and the residue was dissolved into ethyl acetate (500 mL), washed with saturated aqueous solution of ammonium chloride (3×100 mL), brine (100 mL) and dried over anhydrous Na₂SO₄. After filtration, the filtrate was concentrated under reduced pressure and the residue was purified by gradient elution on silica gel (1% to 10% methanol/CH₂Cl₂) to afford the title compound as a mixture of diastereomers. The two diastereomers were separated by Prep-SFC with the following condition: Column: CHIRALPAK AD-H 5*25 cm, 5 um; Mobile Phase A: CO₂: 60%, Mobile Phase B: IPA (0.2% DEA): 40%; Flow rate: 160 mL/min; Detector: UV 254 nm; to afford the faster eluting Isomer 25A (Rt=3.27 min): ¹H NMR (300 MHz, CD₃OD) δ 8.24 (s, 1H), 8.23 (s, 1H), 5.05-4.97 (m, 2H), 4.38 (dd, J=14.4, 3.3 Hz, 1H), 4.23 (dd, J=14.4, 6.9 Hz, 1H), 4.03-3.97 (m, 1H), 3.81-3.77 (m, 1H), 3.56-3.49 (m, 2H), 2.51-2.39 (m, 2H), 1.73-1.69 (m, 1H), 1.53 (s, 3H), 1.50 (s, 3H), 1.28-1.14 (m, 15H), 0.93 (s, 3H), 0.92 (s, 3H); ³¹P NMR (162 MHz, CD₃OD) δ 21.29; LC/MS: [(M+1)]⁺=570.4; and the slower eluting Isomer 25B (Rt=5.41 min): ¹H NMR (300 MHz, CD₃OD) δ 8.20 (s, 1H), 8.18 (s, 1H), 4.97-4.92 (m, 2H), 4.38 (dd, J=14.7, 3.3 Hz, 1H), 4.20 (dd, J=14.4, 7.2 Hz, 1H), 3.97-3.92 (m, 1H), 3.78 (dd, J=12.9, 8.4 Hz, 1H), 3.50 (dd, J=12.9, 8.4 Hz, 1H), 3.38-3.32 (m, 1H), 2.42 (d, J=6.3 Hz, 2H), 1.77-1.71 (m, 1H), 1.42 (s, 3H), 1.38 (s, 3H), 1.23-1.17 (m, 15H), 0.88-0.85 (m, 6H); ³¹P NMR (162 MHz, CD₃OD) δ 22.44; LC/MS: [(M+1)]⁺=570.4.

The compounds in Table 4 were prepared in an analogous fashion to that described for Example 24A and 24B. The column having the heading INT provides the intermediate example compounds used to make each exemplified compound. The diastereoisomers were separated by one of the four listed methods: reverse phase HPLC, chiral HPLC, SFC, or prep TLC. Absolute sterochemistry of the “A” isomer (faster eluting) and “B” isomer (slower eluting) of each example was not determined.

TABLE 4 LC/MS Ex. EXAMPLE STRUCTURE/NAME (M + 1)⁺ INT. 26A and 26B

570.3 and 570.3 C and R isopropyl (3S)-3-(((S)-((((R)-1-(6-amino-9H-purin-9-yl)propan- 2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2- yl)amino)phosphoryl)amino)-butanoate; and isopropyl (3S)-3-(((R)-((((R)-1-(6-amino-9H-purin-9-yl)propan- 2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2- yl)amino)phosphoryl)amino)-butanoate 27A and 27B

570.3 and 570.3 A and R isopropyl (3R)-3-(((S)-((((R)-1-(6-amino-9H-purin-9-yl)propan- 2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2- yl)amino)phosphoryl)amino)-butanoate; and isopropyl (3R)-3-(((R)-(((R)-1-(6-amino-9H-purin-9-yl)propan- 2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2- yl)amino)phosphoryl)amino)-butanoate 28A and 28B

612.4 and 612.4 F and S isopropyl (3S)-3-(((S)-((((R)-1-(6-amino-9H-purin-9-yl)propan- 2-yl)oxy)methyl)((1-(hexyloxy)-2-methyl-1-oxopropan-2- yl)amino)phosphoryl)amino)-4-methylpentanoate; and isopropyl (3S)-3-(((R)-((((R)-1-(6-amino-9H-purin-9-yl)propan- 2-yl)oxy)methyl)((1-(hexyloxy)-2-methyl-1-oxopropan-2- yl)amino)phosphoryl)amino)-4-methylpentanoate

Retention ³¹P NMR shift time Ex. (ppm) Purification conditions (min) 26A 22.19 (162 MHz; Column: Gemini-NX Prep C18, 5 * 25 cm, 23.9 CD₃OD) 5 μm; Mobile Phase A: Water (plus 5 mM 26B 21.81 (162 MHz; NH₄HCO₃); Mobile Phase B: ACN; Flow 24.2 CD₃OD) rate: 90 mL/min; Gradient: 20% to 60% B in 30 min; Detector: 254 nm 27A 18.85 (162 MHz; Column: Gemini-NX Prep C18, 5 * 25 cm, 23.9 CDCl₃) 5 μm; Mobile Phase A: Water (plus 5 mM 27B 18.76 (162 MHz; NH₄HCO₃); Mobile Phase B: ACN; Flow 24.9 CDCl₃) rate: 90 mL/min; Gradient: 20% to 60% B in 30 min; Detector: 254 nm 28A 22.53 (162 MHz; Column: XBridge Prep C18 OBD, 1.9 * 25 19.35 CD₃OD) cm, 10 um; Mobile Phase A: Water (plus 28B 21.33 (162 MHz; 10 mM NH₄HCO₃); Mobile Phase B: 19.9 CD₃OD) ACN; Flow rate: 20 mL/min; Gradient: 35% to 53% B in 24 min; Detector: 254 nm

Example 29

Assessing Antiviral Potency in a Multiple Round HIV-1 Infection Assay (Viking Assay)

The antiviral activity of the tenofovir prodrugs of the Examples herein was assessed in an assay that measures the rate of replication of HIV in cell culture, termed the Viking assay (Viral KINetics in Green cells) and performed as follows. HIV-1 replication was monitored using MT4-gag-GFP clone D3 (hereafter designated MT4-GFP), which are MT-4 cells modified to harbor a GFP reporter gene, the expression of which is dependent on the HIV-1 expressed proteins tat and rev. Productive infection of an MT4-GFP cell with HIV-1 results in GFP expression approximately 24 h post-infection. MT4-GFP cells were maintained at 37° C./5% CO2/90% relative humidity in RPMI 1640 supplemented with 10% fetal bovine serum, 100 U/ml penicillin/streptomycin, and 400 μg/ml G418 to maintain the reporter gene. For infections, MT4-GFP cells were placed in the same medium lacking G418 and infected overnight with HIV-1 (H9/IIIB strain) virus at an approximate multiplicity of infection of 0.01 in the same incubation conditions. Cells were then washed and re-suspended in either RPMI 1640 supplemented with 10% or 50% normal human serum (NHS) at 1.6×10⁵ cells/mL (10% NHS or 50% NHS, respectively). Compound plates were prepared by dispensing compounds dissolved in DMSO into wells of 384 well poly-D-lysine-coated plates (0.2 μl/well) using an ECHO acoustic dispenser. Each compound was tested in a 10-point serial 3-fold dilution (typical final concentrations: 8.4 μM-0.42 nM). Controls included no inhibitor (DMSO only) and a combination of three antiviral agents (efavirenz, indinavir, an in-house integrase strand transfer inhibitor at final concentrations of 4 μM each). Cells were added (504/well) to compound plates and the infected cells were maintained at 37° C./5% CO2/90% relative humidity.

Infected cells were quantified at two time points, ˜48 h and ˜72 h post-infection, by counting the number of green cells in each well using an Acumen eX3 scanner. The increase in the number of green cells over ˜24 h period gives the reproductive ratio, R₀, which is typically 5-15 and has been shown experimentally to be in logarithmic phase (data not shown). Inhibition of R₀ is calculated for each well, and IC₅₀s determined by non-linear 4-parameter curve fitting. Assay IC₅₀ results are shown in Table 5.

Example 30

Prodrug Stability Assay in Bio-Relevant Media

The following assay was employed to evaluate the stability of the prodrugs in simulated gastrointestinal tract conditions. Preparation of fasted state simulated intestinal fluid (FaSSIF) using Phares SIF Powder was carried out according to protocols from Phare Drug Delivery AG (Baselland, Switzerland). For sample preparation, 10 μL stock solutions (10 mM) of prodrug substance in DMSO was added to 990 μL of 0.5 mg/mL Pancreatin solution (Fisher CAS#8049-47-6) in FaSSIF. Two samples were prepared for each compound at initial. If the sample was clear solution at the beginning, ran one sample directly as initial by HPLC; if the sample was not clear at starting, diluted the sample by 100% ACN. Put the other sample under 37° C. and observed the sample at 5 h time-point. At 5 h time point, if the sample was clear solution then performed HPLC analysis directly; if it was not clear solution, diluted the sample by 100% ACN and assayed by HPLC. All the samples were vortexed for 3 min and observed before injection. For the diluted samples, the area will be multiplied by a factor when data analysis. The analysis was carried out with an Agilent 1100 series HPLC with autosampler. The column was usually a Poroshell 120 EC-C18, 4.6×50 mm, 2.7 μm. The flow rate was 1.8 mL/min, and the injection volume was 5 or 10 μL. UV detection was in the range 210-400 nm. The mobile phase consisted of solvent A (water plus 10 mM tetrabutylammonium bromide) and solvent B (acetonitrile) with a gradient of 90% solvent A at 0 min changing to 95% solvent B over 6 min, maintained for 1.5 min, then reverting to 90% solvent A over 1.6 min. The area of the parent in prodrug at 5 h time point was divided by the area of the parent in prodrug at 0 h time point, to generate the % claimed parent ratio, which are summarized in Table 5 for GI Tract stability.

Example 31

Pharmacokinetic Studies in Dogs—In Vivo Dog PK

Prodrugs were administered to beagle dogs through intravenous (IV) and oral (P.O.) administrations in a non-crossover manner. The IV dose was prepared in 20% hydroxypropyl β-cyclodextrin (HPBCD) and was administered via cephalic or saphenous vein. The P.O. dose was prepared in 10% polysorbate 80 (Tween 80) and was administered via gavage.

Blood samples were serially collected following dose administration for up to 48 hr and plasma was separated by centrifugation. The concentrations of prodrugs in dog plasma were determined by a LC-MS/MS assay following a protein precipitation step and addition of an appropriate internal standard (labetalol, imipramine or diclofenac). Quantification was done by determining peak area-ratios of the prodrugs and tenofovir to the internal standard. Additional blood sample(s) was collected following dose administration for up to 24 hr. Peripheral blood mononuclear cells (PBMCs) were isolated by centrifugation, using tubes and reagents specified for such application. The concentrations of tenofovir and/or its phosphate conjugate(s) in PBMCs were determined by an LC-MS/MS assay following a protein precipitation step and addition of an appropriate internal standard (labetalol, imipramine or diclofenac). Quantification was done by determining peak area-ratios of tenofovir and/or its phosphate conjugate(s) to the internal standard.

Pharmacokinetic parameters were obtained using non-compartmental methods (Watson®). The area under the plasma concentration-time curve (AUC_(0-t)) was calculated from the first time point (0 min) up to the last time point with measurable drug concentration using the linear trapezoidal or linear/log-linear trapezoidal rule. The IV plasma clearance was calculated by dividing the dose by AUC_(0-inf). The terminal half-life of elimination was determined by unweighted linear regression analysis of the log-transformed data. The time points for determination of half-life were selected by visual inspection of the data. The volume of distribution at steady state (Vd_(SS)) was obtained from the product of plasma clearance and mean residence time (determined by dividing the area under the first moment curve by the area under the curve). The maximum plasma concentration (C_(max)) and the time at which maximum concentration occurred (T_(max)) were obtained by inspection of the plasma concentration-time data. Absolute oral bioavailability (% F) was determined from dose-adjusted IV and P.O. AUC ratios of the prodrug. Table 5 shows in vivo dog PK data in the form of TFV-DP concentrations (μM) in dog PBMCs at 24 h following a 10 mg/kg P.O. dose of the indicated prodrug.

TABLE 5 Viking, IC₅₀ Viking, IC₅₀ GI Tract In Vivo (10% NHS) (50% NHS) stability Dog PK Example (nM) (nM) (%) (μM)  1 >8403 >8403  2 >8403 >8403  3 7342 >8403  4 6464 >8403  5 >8403 >8403  6A 20.0 59.3 99.5 2.0  6B 257.9 494.3  7A 26.4 44.1 98.7  7B 378 393  8A 26.5 38.2 89.5  8B 439 531  9A 25.3 66.7 99.6  9B 378 800 10A 10.6 97.2 54.8 10B 435 908 11A 21.5 103.5 11B 20.9 68.4 76.4 12A 41.7 119 12B 20.9 63.2 37.7 13A 8.7 56.4 38.7 13B 34.2 174.9 14A 16.6 70.2 38.3 14B 15.7 51.6 60.6 15A 19.6 146 15B 11.7 79.4 65.8 16A 6.1 18.6 12.7 1.3 16B 7.3 28.3 56.2 1.7 17A 6.5 43.0 30.5 17B 2.2 12.0 0 18A 65.0 134 99.2 18B 3809 7120 19A 51.2 194.8 100 19B 3787 >8403 20A 858.6 4105 20B 112.5 431.8 99.3 21A 1458 8403 21B 269.8 836.1 22A 399.9 480.4 22B 83.8 290.8 99.2 23A >8403 >8403 23B 120.6 488.3 101 24A 0.8 4.4 76 37.5 24B 28.9 170 25A 4.7 12.0 99.0 41.9 25B 590 >2000 100 26A 23.3 116.3 26B 1.5 6.8 96.9 23.8 28A 19.1 58.5 28B 2.1 5.7 83 

What is claimed is:
 1. A compound of structural Formula I:

or pharmaceutically acceptable salt thereof, wherein: R¹ and R² are each independently H or —C₁₋₄alkyl; R³ is —C₁₋₁₀alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; R^(A) is an L-amino acid ester residue of formula (i), a D-amino acid ester residue of formula (ii), or a geminally di-substituted amino acid ester residue of formula (iv):

R⁴ is (a) —C₁₋₄alkyl, (b) —C₁₋₄alkyl substituted with —OH, —SH, —SCH₃, —NH₂, —NH—C(═NH)—NH₂, (c) —CH₂-phenyl, (d) —CH₂-phenol, (e) —(CH₂)₁₋₂—COOH, (f) —(CH₂)₁₋₂—CONH₂, (g) —CH₂-1H-indole, (h) —CH₂-imidazole, (i) aryl or (j) heteroaryl; R⁵ and R⁶ are each CH₃; and R⁹ is —C₁₋₁₀alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
 2. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein one of R¹ and R² is H, and the other is H or —C₁₋₄alkyl.
 3. The compound of claim 2 or a pharmaceutically acceptable salt thereof wherein R³ is —C₃₋₈alkyl.
 4. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R^(A) is:

R⁴ is —C₁₋₄alkyl; and R9 is —C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
 5. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R^(A) is:


6. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein: R¹ is H or —C₁₋₄ alkyl; R² is H or —C₁₋₄ alkyl, R³ is —C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; R⁴ is —CH₃; R⁵ and R⁶ are both —CH₃; and R⁹ is —C₁₋₈alkyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
 7. The compound of claim 1 or a pharmaceutically acceptable salt thereof wherein: one of R¹ and R² is H, and the other is methyl or i-propyl; R³ is i-propyl; R⁴ is —CH₃; and R⁹ is —C₃₋₈ alkyl, cyclobutyl, cyclopentyl or cyclohexyl.
 8. The compound of claim 1 that is: 1-methylethyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; 1-methylethyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; 1-methylethyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; 1-methylethyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; 1-methylethyl (3S)-3-{[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2-oxoethyl]amino}phosphoryl]amino}butanoate; 1-methylethyl (3S)-3-{[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2-oxoethyl]amino}phosphoryl]amino}butanoate; 1-methylethyl (3R)-3-{[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2-oxoethyl]amino}phosphoryl]amino}butanoate; 1-methylethyl (3R)-3-{[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(1S)-1-methyl-2-(1-methylethoxy)-2-oxoethyl]amino}phosphoryl]amino}butanoate; 1-methylethyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2R)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; 1-methylethyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2R)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; cyclopentyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; cyclopentyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; cyclobutyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; cyclobutyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; cyclohexyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; cyclohexyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; 2-methylpropyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; 2-methylpropyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; butyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; butyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; pentyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; pentyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; heptyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; heptyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-L-alaninate; isopropyl (3R)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)(((R)-1-cyclobutoxy-1-oxopropan-2-yl)amino)phosphoryl)amino)butanoate; isopropyl (3R)-3-(((R)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)(((R)-1-cyclobutoxy-1-oxopropan-2-yl)amino)phosphoryl)amino)butanoate; 1-methylethyl (3S)-3-{[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(1R)-2-(cyclobutyloxy)-1-methyl-2-oxoethyl]amino}phosphoryl]amino}butanoate; 1-methylethyl (3S)-3-{[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(1R)-2-(cyclobutyloxy)-1-methyl-2-oxoethyl]amino}phosphoryl]amino}butanoate; cyclobutyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; cyclobutyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; cyclohexyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; cyclohexyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; cyclopentyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; cyclopentyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[(2S)-2-methyl-3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; cyclobutyl N—[(S)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; cyclobutyl N—[(R)-{[(1R)-2-(6-amino-9H-purin-9-yl)-1-methylethoxy]methyl}{[3-(1-methylethoxy)-3-oxopropyl]amino}phosphoryl]-D-alaninate; isopropyl (3S)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate; isopropyl (3S)-3-(((R)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate; isopropyl (3S)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((1-isopropoxy-2-methyl-1-oxopropan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate; isopropyl (3S)-3-(((R)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((1-isopropoxy-2-methyl-1-oxopropan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate; isopropyl (3 S)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-butanoate; isopropyl (3S)-3-(((R)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-butanoate; isopropyl (3R)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-butanoate; isopropyl (3R)-3-(((R)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((2-methyl-1-oxo-1-(pentyloxy)propan-2-yl)amino)phosphoryl)amino)-butanoate; isopropyl (3 S)-3-(((S)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((1-(hexyloxy)-2-methyl-1-oxopropan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate; or isopropyl (3S)-3-(((R)—((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)((1-(hexyloxy)-2-methyl-1-oxopropan-2-yl)amino)phosphoryl)amino)-4-methylpentanoate; or a pharmaceutically acceptable salt thereof.
 9. A pharmaceutical composition comprising an effective amount of the compound of claim 1, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
 10. The pharmaceutical composition of claim 9 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 11. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim 1 or a pharmaceutically acceptable salt thereof.
 12. The method of claim 11 wherein the subject is human.
 13. The method of claim 12 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 14. The pharmaceutical composition of claim 9 further comprising an effective amount of one or more additional HIV antiviral agent or agents selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 15. The compound


16. A pharmaceutical composition comprising an effective amount of the compound of claim 15 and a pharmaceutically acceptable carrier.
 17. The pharmaceutical composition of claim 16 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 18. The pharmaceutical composition of claim 17 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 19. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 15. 20. The method of claim 19 wherein the subject is human.
 21. The method of claim 20 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 22. The method of claim 21 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 23. A compound that is a pharmaceutically acceptable salt of


24. A pharmaceutical composition comprising an effective amount of the compound of claim 23 and a pharmaceutically acceptable carrier.
 25. The pharmaceutical composition of claim 24 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 26. The pharmaceutical composition of claim 25 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 27. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 23. 28. The method of claim 27 wherein the subject is human.
 29. The method of claim 28 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 30. The method of claim 29 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 31. The compound


32. A pharmaceutical composition comprising an effective amount of the compound of claim 31 and a pharmaceutically acceptable carrier.
 33. The pharmaceutical composition of claim 32 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 34. The pharmaceutical composition of claim 33 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 35. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 31. 36. The method of claim 35 wherein the subject is human.
 37. The method of claim 36 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 38. The method of claim 37 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 39. A compound that is a pharmaceutically acceptable salt of


40. A pharmaceutical composition comprising an effective amount of the compound of claim 39 and a pharmaceutically acceptable carrier.
 41. The pharmaceutical composition of claim 40 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 42. The pharmaceutical composition of claim 41 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 43. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 39. 44. The method of claim 43 wherein the subject is human.
 45. The method of claim 44 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 46. The method of claim 45 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 47. The compound


48. A pharmaceutical composition comprising an effective amount of the compound of claim 47 and a pharmaceutically acceptable carrier.
 49. The pharmaceutical composition of claim 48 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 50. The pharmaceutical composition of claim 49 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 51. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 47. 52. The method of claim 51 wherein the subject is human.
 53. The method of claim 52 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 54. The method of claim 53 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 55. A compound that is a pharmaceutically acceptable salt of


56. A pharmaceutical composition comprising an effective amount of the compound of claim 55 and a pharmaceutically acceptable carrier.
 57. The pharmaceutical composition of claim 56 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 58. The pharmaceutical composition of claim 57 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 59. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 55. 60. The method of claim 59 wherein the subject is human.
 61. The method of claim 60 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 62. The method of claim 61 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 63. The compound


64. A pharmaceutical composition comprising an effective amount of the compound of claim 63 and a pharmaceutically acceptable carrier.
 65. The pharmaceutical composition of claim 64 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 66. The pharmaceutical composition of claim 65 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 67. A method for the treatment of infection by HIV or for the treatment of delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 63. 68. The method of claim 67 wherein the subject is human.
 69. The method of claim 68 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 70. The method of claim 69 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 71. A compound that is a pharmaceutically acceptable salt of


72. A pharmaceutical composition comprising an effective amount of the compound of claim 71 and a pharmaceutically acceptable carrier.
 73. The pharmaceutical composition of claim 72 further comprising an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 74. The pharmaceutical composition of claim 73 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 75. A method for the treatment of infection by HIV or for the treatment or delay in the onset of AIDS in a subject in need thereof which comprises administering to the subject an effective amount of the compound of claim
 71. 76. The method of claim 75 wherein the subject is human.
 77. The method of claim 76 further comprising administering to the human an effective amount of one or more additional HIV antiviral agent selected from HIV protease inhibitors, HIV integrase inhibitors, non-nucleoside HIV reverse transcriptase inhibitors, nucleoside HIV reverse transcriptase inhibitors, HIV fusion inhibitors and HIV entry inhibitors.
 78. The method of claim 77 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir+lamivudine, abacavir+lamivudine+zidovudine, amprenavir, atazanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz+emtricitabine+tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine+tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine+zidovudine, lopinavir, lopinavir+ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc.
 79. The compound of claim 6, or a pharmaceutically acceptable salt thereof, wherein R^(A) is


80. The compound of claim 7, or a pharmaceutically acceptable salt thereof, wherein R^(A) is


81. The method of claim 13 comprising an effective amount of one or more additional HIV antiviral agent selected from: abacavir, abacavir sulfate, abacavir +lamivudine, abacavir+ lamivudine -F- zidovudine, amprena.vir, ata.zanavir, atazanavir sulfate, AZT, capravirine, darunavir, ddC, ddI, delavirdine, delavirdine mesylate, dolutegravir, doravirine, efavirenz, efavirenz +emtricitabine +tenofovir DF, 4′-ethynyl-2-fluoro-2′-deoxyadenosine, elvitegravir, emtricitabine, emtricitabine H- tenofovir DF, emvirine, enfuvirtide, enteric coated didanosine, etravirine, fosamprenavir calcium, indinavir, indinavir sulfate, lamivudine, lamivudine +zidovudine, lopinavir, lopinavir +ritonavir, maraviroc, nelfinavir, nelfinavir mesylate, nevirapine, PPL-100, raltegravir, rilpivirine, ritonavir, saquinavir, saquinavir mesylate, stavudine, tipranavir and vicriviroc. 